Search term TCGA-BA-7269-01A-11D returned NO results from Exome Somatic dbGENVOC section.
Search term TCGA-BA-7269-01A-11D returned results from TCGA Exome Somatic Variation section.
| DBID | Gene name | Entrez Id | Disease | Chrom | Start | End | Genome change | UCSC Browser | cDNA change | Codon change | Protein change | Variant class | Variant type | Referrence Allele | Tumor Allele | dbSNP ID | Sample Id | Annotation transcript | Transcript strand | Transcript exon | Transcript position | Reference |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| tcga693 | CALHM1 | 255022 | OT-TCGA | chr10 | 105218230 | 105218230 | g.chr10:105218230G>A | chr10:105218230-105218230 | c.279C>T | c.(277-279)ccC>ccT | p.P93P | Silent | SNP | G | A | TCGA-BA-7269-01A-11D | ENST00000329905.5 | - | 1 | 415 | TCGA | |
| tcga694 | VENTX | 27287 | OT-TCGA | chr10 | 135053283 | 135053283 | g.chr10:135053283C>G | chr10:135053283-135053283 | c.345C>G | c.(343-345)taC>taG | p.Y115* | Nonsense_Mutation | SNP | C | G | TCGA-BA-7269-01A-11D | ENST00000325980.9 | + | 2 | 856 | TCGA | |
| tcga695 | PCGF5 | 84333 | OT-TCGA | chr10 | 93038049 | 93038049 | g.chr10:93038049T>G | chr10:93038049-93038049 | c.747T>G | c.(745-747)taT>taG | p.Y249* | Nonsense_Mutation | SNP | T | G | TCGA-BA-7269-01A-11D | ENST00000336126.5 | + | 10 | 979 | TCGA | |
| tcga696 | IDE | 3416 | OT-TCGA | chr10 | 94294475 | 94294475 | g.chr10:94294475T>C | chr10:94294475-94294475 | c.351A>G | c.(349-351)ggA>ggG | p.G117G | Silent | SNP | T | C | TCGA-BA-7269-01A-11D | ENST00000265986.6 | - | 3 | 407 | TCGA | |
| tcga697 | AHNAK | 79026 | OT-TCGA | chr11 | 62296954 | 62296954 | g.chr11:62296954C>A | chr11:62296954-62296954 | c.4935G>T | c.(4933-4935)gaG>gaT | p.E1645D | Missense_Mutation | SNP | C | A | TCGA-BA-7269-01A-11D | ENST00000378024.4 | - | 5 | 5209 | TCGA | |
| tcga698 | RTN3 | 10313 | OT-TCGA | chr11 | 63488185 | 63488185 | g.chr11:63488185C>A | chr11:63488185-63488185 | Intron | SNP | C | A | TCGA-BA-7269-01A-11D | ENST00000537981.1 | + | 2 | 279 | TCGA | ||||
| tcga699 | USP15 | 9958 | OT-TCGA | chr12 | 62715344 | 62715344 | g.chr12:62715344A>G | chr12:62715344-62715344 | c.575A>G | c.(574-576)aAt>aGt | p.N192S | Missense_Mutation | SNP | A | G | TCGA-BA-7269-01A-11D | ENST00000280377.5 | + | 5 | 633 | TCGA | |
| tcga700 | PTPN6 | 5777 | OT-TCGA | chr12 | 7065324 | 7065324 | g.chr12:7065324C>T | chr12:7065324-7065324 | c.864C>T | c.(862-864)atC>atT | p.I288I | Silent | SNP | C | T | TCGA-BA-7269-01A-11D | ENST00000318974.9 | + | 8 | 1108 | TCGA | |
| tcga701 | E2F7 | 144455 | OT-TCGA | chr12 | 77439832 | 77439832 | g.chr12:77439832G>T | chr12:77439832-77439832 | c.815C>A | c.(814-816)cCc>cAc | p.P272H | Missense_Mutation | SNP | G | T | TCGA-BA-7269-01A-11D | ENST00000322886.7 | - | 5 | 1050 | TCGA | |
| tcga702 | SACS | 26278 | OT-TCGA | chr13 | 23942586 | 23942586 | g.chr13:23942586G>C | chr13:23942586-23942586 | c.300C>G | c.(298-300)ctC>ctG | p.L100L | Silent | SNP | G | C | TCGA-BA-7269-01A-11D | ENST00000382292.3 | - | 4 | 573 | TCGA | |
| tcga703 | KLHL1 | 57626 | OT-TCGA | chr13 | 70549922 | 70549922 | g.chr13:70549922G>A | chr13:70549922-70549922 | c.510C>T | c.(508-510)acC>acT | p.T170T | Silent | SNP | G | A | rs369830875 | TCGA-BA-7269-01A-11D | ENST00000377844.4 | - | 2 | 1269 | TCGA |
| tcga704 | ARHGAP5 | 394 | OT-TCGA | chr14 | 32560503 | 32560516 | g.chr14:32560503_32560516delAGAGAAGTTCAGGC | chr14:32560503-32560516 | c.628_641delAGAGAAGTTCAGGC | c.(628-642)agagaagttcaggcafs | p.REVQA210fs | Frame_Shift_Del | DEL | AGAGAAGTTCAGGC | - | rs369093762 | TCGA-BA-7269-01A-11D | ENST00000345122.3 | + | 2 | 943_956 | TCGA |
| tcga705 | CLEC14A | 161198 | OT-TCGA | chr14 | 38724915 | 38724915 | g.chr14:38724915G>A | chr14:38724915-38724915 | c.313C>T | c.(313-315)Ctg>Ttg | p.L105L | Silent | SNP | G | A | TCGA-BA-7269-01A-11D | ENST00000342213.2 | - | 1 | 659 | TCGA | |
| tcga706 | FLRT2 | 23768 | OT-TCGA | chr14 | 86088851 | 86088851 | g.chr14:86088851T>C | chr14:86088851-86088851 | c.993T>C | c.(991-993)tcT>tcC | p.S331S | Silent | SNP | T | C | TCGA-BA-7269-01A-11D | ENST00000330753.4 | + | 2 | 1760 | TCGA | |
| tcga707 | MAP1A | 4130 | OT-TCGA | chr15 | 43821107 | 43821107 | g.chr15:43821107G>A | chr15:43821107-43821107 | c.8150G>A | c.(8149-8151)cGg>cAg | p.R2717Q | Missense_Mutation | SNP | G | A | rs201705385 | TCGA-BA-7269-01A-11D | ENST00000382031.1 | + | 5 | 8181 | TCGA |
| tcga708 | PEAK1 | 79834 | OT-TCGA | chr15 | 77474216 | 77474216 | g.chr15:77474216T>C | chr15:77474216-77474216 | c.53A>G | c.(52-54)aAg>aGg | p.K18R | Missense_Mutation | SNP | T | C | TCGA-BA-7269-01A-11D | ENST00000560626.2 | - | 4 | 528 | TCGA | |
| tcga709 | NFATC2IP | 84901 | OT-TCGA | chr16 | 28975123 | 28975123 | g.chr16:28975123G>T | chr16:28975123-28975123 | c.1199G>T | c.(1198-1200)gGc>gTc | p.G400V | Missense_Mutation | SNP | G | T | TCGA-BA-7269-01A-11D | ENST00000320805.4 | + | 8 | 1274 | TCGA | |
| tcga710 | ANKS3 | 124401 | OT-TCGA | chr16 | 4774826 | 4774826 | g.chr16:4774826C>T | chr16:4774826-4774826 | c.498G>A | c.(496-498)ccG>ccA | p.P166P | Silent | SNP | C | T | TCGA-BA-7269-01A-11D | ENST00000304283.4 | - | 6 | 792 | TCGA | |
| tcga711 | C16orf71 | 146562 | OT-TCGA | chr16 | 4793097 | 4793097 | g.chr16:4793097A>C | chr16:4793097-4793097 | c.879A>C | c.(877-879)gaA>gaC | p.E293D | Missense_Mutation | SNP | A | C | TCGA-BA-7269-01A-11D | ENST00000590191.1 | + | 5 | 1149 | TCGA | |
| tcga712 | CDH11 | 1009 | OT-TCGA | chr16 | 64984856 | 64984856 | g.chr16:64984856G>A | chr16:64984856-64984856 | c.1708C>T | c.(1708-1710)Ctg>Ttg | p.L570L | Silent | SNP | G | A | rs142957030 | TCGA-BA-7269-01A-11D | ENST00000268603.4 | - | 12 | 2323 | TCGA |
| tcga713 | RANBP10 | 57610 | OT-TCGA | chr16 | 67761784 | 67761784 | g.chr16:67761784C>T | chr16:67761784-67761784 | c.1490G>A | c.(1489-1491)cGg>cAg | p.R497Q | Missense_Mutation | SNP | C | T | TCGA-BA-7269-01A-11D | ENST00000317506.3 | - | 12 | 1605 | TCGA | |
| tcga714 | RP11-252A24.2 | 0 | OT-TCGA | chr16 | 74372351 | 74372351 | g.chr16:74372351C>G | chr16:74372351-74372351 | ncRNA | SNP | C | G | TCGA-BA-7269-01A-11D | ENST00000429810.2 | - | 0 | 1845 | TCGA | ||||
| tcga715 | RAI1 | 10743 | OT-TCGA | chr17 | 17697704 | 17697704 | g.chr17:17697704G>T | chr17:17697704-17697704 | c.1442G>T | c.(1441-1443)tGc>tTc | p.C481F | Missense_Mutation | SNP | G | T | TCGA-BA-7269-01A-11D | ENST00000353383.1 | + | 3 | 1911 | TCGA | |
| tcga716 | CDC6 | 990 | OT-TCGA | chr17 | 38450241 | 38450241 | g.chr17:38450241A>G | chr17:38450241-38450241 | c.876A>G | c.(874-876)aaA>aaG | p.K292K | Silent | SNP | A | G | TCGA-BA-7269-01A-11D | ENST00000209728.4 | + | 6 | 1347 | TCGA | |
| tcga717 | TP53 | 7157 | OT-TCGA | chr17 | 7578180 | 7578181 | g.chr17:7578180_7578181insT | chr17:7578180-7578181 | c.668_669insA | c.(667-669)cctfs | p.P223fs | Frame_Shift_Ins | INS | - | T | rs138983188 | TCGA-BA-7269-01A-11D | ENST00000269305.4 | - | 6 | 857_858 | TCGA |
| tcga718 | DSEL | 92126 | OT-TCGA | chr18 | 65180850 | 65180850 | g.chr18:65180850G>T | chr18:65180850-65180850 | c.1026C>A | c.(1024-1026)tcC>tcA | p.S342S | Silent | SNP | G | T | TCGA-BA-7269-01A-11D | ENST00000310045.7 | - | 2 | 2499 | TCGA | |
| tcga719 | KEAP1 | 9817 | OT-TCGA | chr19 | 10597411 | 10597411 | g.chr19:10597411T>C | chr19:10597411-10597411 | c.1792A>G | c.(1792-1794)Aca>Gca | p.T598A | Missense_Mutation | SNP | T | C | TCGA-BA-7269-01A-11D | ENST00000171111.5 | - | 6 | 2339 | TCGA | |
| tcga720 | ZNF709 | 163051 | OT-TCGA | chr19 | 12575387 | 12575387 | g.chr19:12575387C>A | chr19:12575387-12575387 | c.1349G>T | c.(1348-1350)tGt>tTt | p.C450F | Missense_Mutation | SNP | C | A | TCGA-BA-7269-01A-11D | ENST00000397732.3 | - | 4 | 1520 | TCGA | |
| tcga721 | ZNF302 | 55900 | OT-TCGA | chr19 | 35175566 | 35175566 | g.chr19:35175566A>G | chr19:35175566-35175566 | c.756A>G | c.(754-756)aaA>aaG | p.K252K | Silent | SNP | A | G | TCGA-BA-7269-01A-11D | ENST00000446502.2 | + | 6 | 964 | TCGA | |
| tcga722 | AXL | 558 | OT-TCGA | chr19 | 41749592 | 41749592 | g.chr19:41749592G>A | chr19:41749592-41749592 | c.1517G>A | c.(1516-1518)cGt>cAt | p.R506H | Missense_Mutation | SNP | G | A | TCGA-BA-7269-01A-11D | ENST00000301178.4 | + | 12 | 1707 | TCGA | |
| tcga723 | ZNF230 | 7773 | OT-TCGA | chr19 | 44516645 | 44516646 | g.chr19:44516645_44516646insAG | chr19:44516645-44516646 | 3'UTR | INS | - | AG | TCGA-BA-7269-01A-11D | ENST00000429154.2 | + | 0 | 2682_2683 | TCGA | ||||
| tcga724 | SLC8A2 | 6543 | OT-TCGA | chr19 | 47941206 | 47941206 | g.chr19:47941206G>A | chr19:47941206-47941206 | c.1910C>T | c.(1909-1911)gCc>gTc | p.A637V | Missense_Mutation | SNP | G | A | TCGA-BA-7269-01A-11D | ENST00000236877.6 | - | 7 | 2305 | TCGA | |
| tcga725 | SIGLEC12 | 89858 | OT-TCGA | chr19 | 52003547 | 52003547 | g.chr19:52003547C>A | chr19:52003547-52003547 | c.435G>T | c.(433-435)caG>caT | p.Q145H | Missense_Mutation | SNP | C | A | TCGA-BA-7269-01A-11D | ENST00000291707.3 | - | 2 | 490 | TCGA | |
| tcga726 | MIR518F | 574472 | OT-TCGA | chr19 | 54206072 | 54206072 | g.chr19:54206072G>C | chr19:54206072-54206072 | ncRNA | SNP | G | C | TCGA-BA-7269-01A-11D | ENST00000384973.1 | + | 0 | 87 | TCGA | ||||
| tcga727 | TFPT | 29844 | OT-TCGA | chr19 | 54611775 | 54611775 | g.chr19:54611775G>A | chr19:54611775-54611775 | Intron | SNP | G | A | TCGA-BA-7269-01A-11D | ENST00000391759.1 | - | 4 | 759 | TCGA | ||||
| tcga728 | BRSK1 | 84446 | OT-TCGA | chr19 | 55823324 | 55823324 | g.chr19:55823324G>A | chr19:55823324-55823324 | c.1310G>A | c.(1309-1311)cGa>cAa | p.R437Q | Missense_Mutation | SNP | G | A | TCGA-BA-7269-01A-11D | ENST00000326848.7 | + | 11 | 1518 | TCGA | |
| tcga729 | OLFM3 | 118427 | OT-TCGA | chr1 | 102271700 | 102271700 | g.chr1:102271700C>A | chr1:102271700-102271700 | c.691G>T | c.(691-693)Gtc>Ttc | p.V231F | Missense_Mutation | SNP | C | A | TCGA-BA-7269-01A-11D | ENST00000338858.5 | - | 5 | 690 | TCGA | |
| tcga730 | RFX5 | 5993 | OT-TCGA | chr1 | 151316211 | 151316211 | g.chr1:151316211G>T | chr1:151316211-151316211 | c.703C>A | c.(703-705)Ctc>Atc | p.L235I | Missense_Mutation | SNP | G | T | TCGA-BA-7269-01A-11D | ENST00000290524.4 | - | 9 | 881 | TCGA | |
| tcga731 | ATP8B2 | 57198 | OT-TCGA | chr1 | 154303375 | 154303378 | g.chr1:154303375_154303378delACTT | chr1:154303375-154303378 | c.274_277delACTT | c.(274-279)acttacfs | p.TY92fs | Frame_Shift_Del | DEL | ACTT | - | TCGA-BA-7269-01A-11D | ENST00000368489.3 | + | 4 | 274_277 | TCGA | |
| tcga732 | CD5L | 922 | OT-TCGA | chr1 | 157811469 | 157811469 | g.chr1:157811469A>G | chr1:157811469-157811469 | c.23T>C | c.(22-24)aTc>aCc | p.I8T | Missense_Mutation | SNP | A | G | TCGA-BA-7269-01A-11D | ENST00000368174.4 | - | 1 | 119 | TCGA | |
| tcga733 | PAPPA2 | 60676 | OT-TCGA | chr1 | 176738821 | 176738821 | g.chr1:176738821G>T | chr1:176738821-176738821 | c.4402G>T | c.(4402-4404)Gac>Tac | p.D1468Y | Missense_Mutation | SNP | G | T | rs371564283 | TCGA-BA-7269-01A-11D | ENST00000367662.3 | + | 16 | 5566 | TCGA |
| tcga734 | ASPM | 259266 | OT-TCGA | chr1 | 197072273 | 197072273 | g.chr1:197072273C>A | chr1:197072273-197072273 | c.6108G>T | c.(6106-6108)gtG>gtT | p.V2036V | Silent | SNP | C | A | TCGA-BA-7269-01A-11D | ENST00000367409.4 | - | 18 | 6364 | TCGA | |
| tcga735 | ATP2B4 | 493 | OT-TCGA | chr1 | 203682333 | 203682333 | g.chr1:203682333G>C | chr1:203682333-203682333 | c.2252G>C | c.(2251-2253)cGg>cCg | p.R751P | Missense_Mutation | SNP | G | C | TCGA-BA-7269-01A-11D | ENST00000357681.5 | + | 14 | 3375 | TCGA | |
| tcga736 | LRRN2 | 10446 | OT-TCGA | chr1 | 204587686 | 204587686 | g.chr1:204587686C>T | chr1:204587686-204587686 | c.1435G>A | c.(1435-1437)Gag>Aag | p.E479K | Missense_Mutation | SNP | C | T | TCGA-BA-7269-01A-11D | ENST00000367175.1 | - | 1 | 3647 | TCGA | |
| tcga737 | RPS6KC1 | 26750 | OT-TCGA | chr1 | 213436154 | 213436154 | g.chr1:213436154C>T | chr1:213436154-213436154 | c.3049C>T | c.(3049-3051)Caa>Taa | p.Q1017* | Nonsense_Mutation | SNP | C | T | rs367780807 | TCGA-BA-7269-01A-11D | ENST00000366959.3 | + | 13 | 3199 | TCGA |
| tcga738 | LYST | 1130 | OT-TCGA | chr1 | 235952058 | 235952058 | g.chr1:235952058G>T | chr1:235952058-235952058 | c.4631C>A | c.(4630-4632)tCc>tAc | p.S1544Y | Missense_Mutation | SNP | G | T | TCGA-BA-7269-01A-11D | ENST00000389794.3 | - | 13 | 4805 | TCGA | |
| tcga739 | OR2M2 | 391194 | OT-TCGA | chr1 | 248344299 | 248344299 | g.chr1:248344299A>G | chr1:248344299-248344299 | c.1012A>G | c.(1012-1014)Aaa>Gaa | p.K338E | Missense_Mutation | SNP | A | G | TCGA-BA-7269-01A-11D | ENST00000359682.2 | + | 1 | 1012 | TCGA | |
| tcga740 | ACTRT2 | 140625 | OT-TCGA | chr1 | 2939160 | 2939160 | g.chr1:2939160G>A | chr1:2939160-2939160 | c.910G>A | c.(910-912)Ggc>Agc | p.G304S | Missense_Mutation | SNP | G | A | TCGA-BA-7269-01A-11D | ENST00000378404.2 | + | 1 | 1115 | TCGA | |
| tcga741 | TMEM39B | 55116 | OT-TCGA | chr1 | 32566231 | 32566231 | g.chr1:32566231G>T | chr1:32566231-32566231 | Intron | SNP | G | T | TCGA-BA-7269-01A-11D | ENST00000336294.5 | + | 8 | 1382 | TCGA | ||||
| tcga742 | PABPC4 | 8761 | OT-TCGA | chr1 | 40034520 | 40034520 | g.chr1:40034520T>A | chr1:40034520-40034520 | c.830A>T | c.(829-831)aAa>aTa | p.K277I | Missense_Mutation | SNP | T | A | TCGA-BA-7269-01A-11D | ENST00000372862.3 | - | 6 | 1131 | TCGA | |
| tcga743 | CMPK1 | 51727 | OT-TCGA | chr1 | 47834266 | 47834266 | g.chr1:47834266A>G | chr1:47834266-47834266 | c.297A>G | c.(295-297)atA>atG | p.I99M | Missense_Mutation | SNP | A | G | TCGA-BA-7269-01A-11D | ENST00000371873.5 | + | 2 | 446 | TCGA | |
| tcga744 | TCEANC2 | 127428 | OT-TCGA | chr1 | 54562121 | 54562121 | g.chr1:54562121C>T | chr1:54562121-54562121 | c.602C>T | c.(601-603)aCg>aTg | p.T201M | Missense_Mutation | SNP | C | T | TCGA-BA-7269-01A-11D | ENST00000234827.1 | + | 5 | 802 | TCGA | |
| tcga745 | CAMTA1 | 23261 | OT-TCGA | chr1 | 7798137 | 7798137 | g.chr1:7798137G>A | chr1:7798137-7798137 | c.3777G>A | c.(3775-3777)aaG>aaA | p.K1259K | Silent | SNP | G | A | TCGA-BA-7269-01A-11D | ENST00000303635.7 | + | 16 | 3984 | TCGA | |
| tcga746 | CAMTA1 | 23261 | OT-TCGA | chr1 | 7798138 | 7798138 | g.chr1:7798138C>T | chr1:7798138-7798138 | c.3778C>T | c.(3778-3780)Ctg>Ttg | p.L1260L | Silent | SNP | C | T | TCGA-BA-7269-01A-11D | ENST00000303635.7 | + | 16 | 3985 | TCGA | |
| tcga747 | FUBP1 | 8880 | OT-TCGA | chr1 | 78430374 | 78430374 | g.chr1:78430374C>T | chr1:78430374-78430374 | c.794G>A | c.(793-795)cGg>cAg | p.R265Q | Missense_Mutation | SNP | C | T | TCGA-BA-7269-01A-11D | ENST00000370768.2 | - | 10 | 875 | TCGA | |
| tcga748 | XRN2 | 22803 | OT-TCGA | chr20 | 21312236 | 21312236 | g.chr20:21312236A>G | chr20:21312236-21312236 | c.614A>G | c.(613-615)gAa>gGa | p.E205G | Missense_Mutation | SNP | A | G | TCGA-BA-7269-01A-11D | ENST00000377191.3 | + | 7 | 709 | TCGA | |
| tcga749 | SLC23A2 | 9962 | OT-TCGA | chr20 | 4880210 | 4880210 | g.chr20:4880210A>G | chr20:4880210-4880210 | c.473T>C | c.(472-474)tTt>tCt | p.F158S | Missense_Mutation | SNP | A | G | TCGA-BA-7269-01A-11D | ENST00000379333.1 | - | 6 | 865 | TCGA | |
| tcga750 | MRPL39 | 54148 | OT-TCGA | chr21 | 26978860 | 26978860 | g.chr21:26978860G>C | chr21:26978860-26978860 | c.181C>G | c.(181-183)Cga>Gga | p.R61G | Missense_Mutation | SNP | G | C | TCGA-BA-7269-01A-11D | ENST00000307301.7 | - | 2 | 222 | TCGA | |
| tcga751 | APP | 351 | OT-TCGA | chr21 | 27394285 | 27394285 | g.chr21:27394285C>T | chr21:27394285-27394285 | c.736G>A | c.(736-738)Gag>Aag | p.E246K | Missense_Mutation | SNP | C | T | rs147485129 | TCGA-BA-7269-01A-11D | ENST00000346798.3 | - | 6 | 769 | TCGA |
| tcga752 | NEFH | 4744 | OT-TCGA | chr22 | 29879403 | 29879403 | g.chr22:29879403C>T | chr22:29879403-29879403 | c.923C>T | c.(922-924)aCa>aTa | p.T308I | Missense_Mutation | SNP | C | T | TCGA-BA-7269-01A-11D | ENST00000310624.6 | + | 2 | 956 | TCGA | |
| tcga753 | SSTR3 | 6753 | OT-TCGA | chr22 | 37603361 | 37603361 | g.chr22:37603361C>T | chr22:37603361-37603361 | c.482G>A | c.(481-483)cGc>cAc | p.R161H | Missense_Mutation | SNP | C | T | rs371788740 | TCGA-BA-7269-01A-11D | ENST00000328544.3 | - | 2 | 1015 | TCGA |
| tcga754 | APOBEC3B | 9582 | OT-TCGA | chr22 | 39387518 | 39387518 | g.chr22:39387518A>G | chr22:39387518-39387518 | c.830A>G | c.(829-831)cAc>cGc | p.H277R | Missense_Mutation | SNP | A | G | TCGA-BA-7269-01A-11D | ENST00000407298.3 | + | 6 | 937 | TCGA | |
| tcga755 | PLEKHB2 | 55041 | OT-TCGA | chr2 | 131976382 | 131976382 | g.chr2:131976382G>A | chr2:131976382-131976382 | Intron | SNP | G | A | TCGA-BA-7269-01A-11D | ENST00000404460.1 | + | 6 | 477 | TCGA | ||||
| tcga756 | KYNU | 8942 | OT-TCGA | chr2 | 143712382 | 143712382 | g.chr2:143712382C>G | chr2:143712382-143712382 | c.377C>G | c.(376-378)gCc>gGc | p.A126G | Missense_Mutation | SNP | C | G | TCGA-BA-7269-01A-11D | ENST00000264170.4 | + | 5 | 635 | TCGA | |
| tcga757 | NFE2L2 | 4780 | OT-TCGA | chr2 | 178096545 | 178096545 | g.chr2:178096545G>C | chr2:178096545-178096545 | c.717C>G | c.(715-717)gaC>gaG | p.D239E | Missense_Mutation | SNP | G | C | TCGA-BA-7269-01A-11D | ENST00000446151.2 | - | 5 | 889 | TCGA | |
| tcga758 | TTN | 7273 | OT-TCGA | chr2 | 179471858 | 179471858 | g.chr2:179471858A>G | chr2:179471858-179471858 | c.53471T>C | c.(53470-53472)aTc>aCc | p.I17824T | Missense_Mutation | SNP | A | G | TCGA-BA-7269-01A-11D | ENST00000589042.1 | - | 278 | 53695 | TCGA | |
| tcga759 | ZNF142 | 7701 | OT-TCGA | chr2 | 219510940 | 219510940 | g.chr2:219510940T>A | chr2:219510940-219510940 | c.1405A>T | c.(1405-1407)Aag>Tag | p.K469* | Nonsense_Mutation | SNP | T | A | TCGA-BA-7269-01A-11D | ENST00000449707.1 | - | 7 | 1826 | TCGA | |
| tcga760 | COPS7B | 64708 | OT-TCGA | chr2 | 232653363 | 232653363 | g.chr2:232653363C>A | chr2:232653363-232653363 | Intron | SNP | C | A | TCGA-BA-7269-01A-11D | ENST00000409295.1 | + | 2 | 206 | TCGA | ||||
| tcga761 | LCLAT1 | 253558 | OT-TCGA | chr2 | 30863047 | 30863047 | g.chr2:30863047G>C | chr2:30863047-30863047 | c.693G>C | c.(691-693)gaG>gaC | p.E231D | Missense_Mutation | SNP | G | C | TCGA-BA-7269-01A-11D | ENST00000379509.3 | + | 6 | 845 | TCGA | |
| tcga762 | CNNM4 | 26504 | OT-TCGA | chr2 | 97427416 | 97427416 | g.chr2:97427416G>A | chr2:97427416-97427416 | c.680G>A | c.(679-681)cGc>cAc | p.R227H | Missense_Mutation | SNP | G | A | TCGA-BA-7269-01A-11D | ENST00000377075.2 | + | 1 | 778 | TCGA | |
| tcga763 | VWA3B | 200403 | OT-TCGA | chr2 | 98852910 | 98852910 | g.chr2:98852910C>T | chr2:98852910-98852910 | c.2486C>T | c.(2485-2487)aCg>aTg | p.T829M | Missense_Mutation | SNP | C | T | rs375038927 | TCGA-BA-7269-01A-11D | ENST00000477737.1 | + | 18 | 2690 | TCGA |
| tcga764 | INPP4A | 3631 | OT-TCGA | chr2 | 99160454 | 99160454 | g.chr2:99160454C>T | chr2:99160454-99160454 | c.933C>T | c.(931-933)gaC>gaT | p.D311D | Silent | SNP | C | T | TCGA-BA-7269-01A-11D | ENST00000409016.4 | + | 11 | 1330 | TCGA | |
| tcga765 | FANCD2 | 2177 | OT-TCGA | chr3 | 10122836 | 10122836 | g.chr3:10122836A>G | chr3:10122836-10122836 | c.3029A>G | c.(3028-3030)cAa>cGa | p.Q1010R | Missense_Mutation | SNP | A | G | rs376836572 | TCGA-BA-7269-01A-11D | ENST00000419585.1 | + | 31 | 3190 | TCGA |
| tcga766 | SLC12A8 | 84561 | OT-TCGA | chr3 | 124906105 | 124906105 | g.chr3:124906105G>A | chr3:124906105-124906105 | c.366C>T | c.(364-366)atC>atT | p.I122I | Silent | SNP | G | A | TCGA-BA-7269-01A-11D | ENST00000393469.4 | - | 3 | 415 | TCGA | |
| tcga767 | CAND2 | 23066 | OT-TCGA | chr3 | 12858258 | 12858258 | g.chr3:12858258C>G | chr3:12858258-12858258 | c.1827C>G | c.(1825-1827)gaC>gaG | p.D609E | Missense_Mutation | SNP | C | G | TCGA-BA-7269-01A-11D | ENST00000456430.2 | + | 10 | 1868 | TCGA | |
| tcga768 | PLD1 | 5337 | OT-TCGA | chr3 | 171394572 | 171394572 | g.chr3:171394572G>A | chr3:171394572-171394572 | c.1934C>T | c.(1933-1935)tCt>tTt | p.S645F | Missense_Mutation | SNP | G | A | TCGA-BA-7269-01A-11D | ENST00000356327.5 | - | 17 | 2004 | TCGA | |
| tcga769 | SLC4A7 | 9497 | OT-TCGA | chr3 | 27477926 | 27477926 | g.chr3:27477926C>A | chr3:27477926-27477926 | c.530G>T | c.(529-531)gGa>gTa | p.G177V | Missense_Mutation | SNP | C | A | TCGA-BA-7269-01A-11D | ENST00000455077.1 | - | 5 | 750 | TCGA | |
| tcga770 | SETD2 | 29072 | OT-TCGA | chr3 | 47162207 | 47162207 | g.chr3:47162207C>G | chr3:47162207-47162207 | c.3919G>C | c.(3919-3921)Gat>Cat | p.D1307H | Missense_Mutation | SNP | C | G | TCGA-BA-7269-01A-11D | ENST00000409792.3 | - | 3 | 3961 | TCGA | |
| tcga771 | TBCK | 93627 | OT-TCGA | chr4 | 107016738 | 107016738 | g.chr4:107016738T>G | chr4:107016738-107016738 | c.2472A>C | c.(2470-2472)gcA>gcC | p.A824A | Silent | SNP | T | G | TCGA-BA-7269-01A-11D | ENST00000273980.5 | - | 26 | 2919 | TCGA | |
| tcga772 | KIAA0922 | 23240 | OT-TCGA | chr4 | 154525199 | 154525199 | g.chr4:154525199G>A | chr4:154525199-154525199 | c.3035G>A | c.(3034-3036)aGc>aAc | p.S1012N | Missense_Mutation | SNP | G | A | TCGA-BA-7269-01A-11D | ENST00000409959.3 | + | 25 | 3084 | TCGA | |
| tcga773 | GALNTL6 | 442117 | OT-TCGA | chr4 | 172735665 | 172735665 | g.chr4:172735665G>T | chr4:172735665-172735665 | 5'UTR | SNP | G | T | TCGA-BA-7269-01A-11D | ENST00000506823.1 | + | 0 | 591 | TCGA | ||||
| tcga774 | FAT1 | 2195 | OT-TCGA | chr4 | 187628726 | 187628732 | g.chr4:187628726_187628732delCAGTTTT | chr4:187628726-187628732 | c.2250_2256delAAAACTG | c.(2248-2256)ggaaaactgfs | p.GKL750fs | Frame_Shift_Del | DEL | CAGTTTT | - | TCGA-BA-7269-01A-11D | ENST00000441802.2 | - | 2 | 2459_2465 | TCGA | |
| tcga775 | UGT2B4 | 7363 | OT-TCGA | chr4 | 70360857 | 70360857 | g.chr4:70360857A>G | chr4:70360857-70360857 | - | Splice_Site | SNP | A | G | rs377159596 | TCGA-BA-7269-01A-11D | ENST00000305107.6 | - | 1 | 768 | TCGA | ||
| tcga776 | SPP1 | 6696 | OT-TCGA | chr4 | 88904092 | 88904092 | g.chr4:88904092delA | chr4:88904092-88904092 | 3'UTR | DEL | A | - | TCGA-BA-7269-01A-11D | ENST00000395080.3 | + | 0 | 1116 | TCGA | ||||
| tcga777 | PCDHA12 | 56137 | OT-TCGA | chr5 | 140256690 | 140256690 | g.chr5:140256690C>G | chr5:140256690-140256690 | c.1633C>G | c.(1633-1635)Ctg>Gtg | p.L545V | Missense_Mutation | SNP | C | G | TCGA-BA-7269-01A-11D | ENST00000398631.2 | + | 1 | 1633 | TCGA | |
| tcga778 | PCDHGB6 | 56100 | OT-TCGA | chr5 | 140788292 | 140788292 | g.chr5:140788292A>C | chr5:140788292-140788292 | c.523A>C | c.(523-525)Aat>Cat | p.N175H | Missense_Mutation | SNP | A | C | TCGA-BA-7269-01A-11D | ENST00000520790.1 | + | 1 | 523 | TCGA | |
| tcga779 | FAM71B | 153745 | OT-TCGA | chr5 | 156590665 | 156590665 | g.chr5:156590665G>A | chr5:156590665-156590665 | c.611C>T | c.(610-612)gCa>gTa | p.A204V | Missense_Mutation | SNP | G | A | TCGA-BA-7269-01A-11D | ENST00000302938.4 | - | 2 | 706 | TCGA | |
| tcga780 | FAM71B | 153745 | OT-TCGA | chr5 | 156590666 | 156590666 | g.chr5:156590666C>A | chr5:156590666-156590666 | c.610G>T | c.(610-612)Gca>Tca | p.A204S | Missense_Mutation | SNP | C | A | TCGA-BA-7269-01A-11D | ENST00000302938.4 | - | 2 | 705 | TCGA | |
| tcga781 | TTC37 | 9652 | OT-TCGA | chr5 | 94820469 | 94820469 | g.chr5:94820469C>G | chr5:94820469-94820469 | c.4012G>C | c.(4012-4014)Gac>Cac | p.D1338H | Missense_Mutation | SNP | C | G | TCGA-BA-7269-01A-11D | ENST00000358746.2 | - | 38 | 4310 | TCGA | |
| tcga782 | SIM1 | 6492 | OT-TCGA | chr6 | 100898154 | 100898154 | g.chr6:100898154C>T | chr6:100898154-100898154 | c.337G>A | c.(337-339)Ggt>Agt | p.G113S | Missense_Mutation | SNP | C | T | TCGA-BA-7269-01A-11D | ENST00000369208.3 | - | 4 | 1119 | TCGA | |
| tcga783 | LRP11 | 84918 | OT-TCGA | chr6 | 150174158 | 150174158 | g.chr6:150174158T>C | chr6:150174158-150174158 | c.752A>G | c.(751-753)gAc>gGc | p.D251G | Missense_Mutation | SNP | T | C | TCGA-BA-7269-01A-11D | ENST00000239367.2 | - | 2 | 757 | TCGA | |
| tcga784 | SCAND3 | 0 | OT-TCGA | chr6 | 28540656 | 28540656 | g.chr6:28540656C>A | chr6:28540656-28540656 | c.3010G>T | c.(3010-3012)Gaa>Taa | p.E1004* | Nonsense_Mutation | SNP | C | A | TCGA-BA-7269-01A-11D | ENST00000452236.2 | - | 4 | 3627 | TCGA | |
| tcga785 | HLA-F | 3134 | OT-TCGA | chr6 | 29692932 | 29692932 | g.chr6:29692932G>C | chr6:29692932-29692932 | c.735G>C | c.(733-735)caG>caC | p.Q245H | Missense_Mutation | SNP | G | C | TCGA-BA-7269-01A-11D | ENST00000376861.1 | + | 5 | 1119 | TCGA | |
| tcga786 | NEU1 | 4758 | OT-TCGA | chr6 | 31827476 | 31827476 | g.chr6:31827476C>T | chr6:31827476-31827476 | 3'UTR | SNP | C | T | TCGA-BA-7269-01A-11D | ENST00000375631.4 | - | 0 | 1397 | TCGA | ||||
| tcga787 | HLA-DMB | 3109 | OT-TCGA | chr6 | 32906490 | 32906490 | g.chr6:32906490G>A | chr6:32906490-32906490 | c.308C>T | c.(307-309)cCc>cTc | p.P103L | Missense_Mutation | SNP | G | A | TCGA-BA-7269-01A-11D | ENST00000418107.2 | - | 2 | 570 | TCGA | |
| tcga788 | ECI2 | 10455 | OT-TCGA | chr6 | 4135788 | 4135788 | g.chr6:4135788T>C | chr6:4135788-4135788 | c.7A>G | c.(7-9)Atg>Gtg | p.M3V | Missense_Mutation | SNP | T | C | TCGA-BA-7269-01A-11D | ENST00000380118.3 | - | 1 | 43 | TCGA | |
| tcga789 | PEX6 | 5190 | OT-TCGA | chr6 | 42934376 | 42934376 | g.chr6:42934376C>T | chr6:42934376-42934376 | c.1981G>A | c.(1981-1983)Gag>Aag | p.E661K | Missense_Mutation | SNP | C | T | TCGA-BA-7269-01A-11D | ENST00000304611.8 | - | 10 | 2050 | TCGA | |
| tcga790 | PAQR8 | 85315 | OT-TCGA | chr6 | 52268767 | 52268767 | g.chr6:52268767C>A | chr6:52268767-52268767 | c.756C>A | c.(754-756)atC>atA | p.I252I | Silent | SNP | C | A | TCGA-BA-7269-01A-11D | ENST00000442253.2 | + | 2 | 930 | TCGA | |
| tcga791 | GCM1 | 8521 | OT-TCGA | chr6 | 52993147 | 52993147 | g.chr6:52993147G>A | chr6:52993147-52993147 | c.1168C>T | c.(1168-1170)Ctc>Ttc | p.L390F | Missense_Mutation | SNP | G | A | TCGA-BA-7269-01A-11D | ENST00000259803.7 | - | 6 | 1379 | TCGA | |
| tcga792 | FBXL4 | 26235 | OT-TCGA | chr6 | 99374830 | 99374830 | g.chr6:99374830G>C | chr6:99374830-99374830 | c.35C>G | c.(34-36)aCc>aGc | p.T12S | Missense_Mutation | SNP | G | C | TCGA-BA-7269-01A-11D | ENST00000369244.2 | - | 4 | 463 | TCGA | |
| tcga793 | FBXO24 | 26261 | OT-TCGA | chr7 | 100198322 | 100198322 | g.chr7:100198322A>G | chr7:100198322-100198322 | c.1543A>G | c.(1543-1545)Atg>Gtg | p.M515V | Missense_Mutation | SNP | A | G | TCGA-BA-7269-01A-11D | ENST00000241071.6 | + | 10 | 1865 | TCGA | |
| tcga794 | CCT6P1 | 643253 | OT-TCGA | chr7 | 65224177 | 65224177 | g.chr7:65224177T>C | chr7:65224177-65224177 | ncRNA | SNP | T | C | TCGA-BA-7269-01A-11D | ENST00000442266.1 | + | 0 | 814 | TCGA | ||||
| tcga795 | STEAP4 | 79689 | OT-TCGA | chr7 | 87910314 | 87910314 | g.chr7:87910314C>T | chr7:87910314-87910314 | c.1065G>A | c.(1063-1065)ggG>ggA | p.G355G | Silent | SNP | C | T | rs375955638 | TCGA-BA-7269-01A-11D | ENST00000380079.4 | - | 4 | 1166 | TCGA |
| tcga796 | TRRAP | 8295 | OT-TCGA | chr7 | 98608797 | 98608797 | g.chr7:98608797C>A | chr7:98608797-98608797 | c.10986C>A | c.(10984-10986)acC>acA | p.T3662T | Silent | SNP | C | A | TCGA-BA-7269-01A-11D | ENST00000446306.3 | + | 68 | 11047 | TCGA | |
| tcga797 | CSMD1 | 64478 | OT-TCGA | chr8 | 3432474 | 3432474 | g.chr8:3432474G>A | chr8:3432474-3432474 | c.1340C>T | c.(1339-1341)cCg>cTg | p.P447L | Missense_Mutation | SNP | G | A | TCGA-BA-7269-01A-11D | ENST00000520002.1 | - | 11 | 1895 | TCGA | |
| tcga798 | GDF6 | 392255 | OT-TCGA | chr8 | 97156765 | 97156765 | g.chr8:97156765G>A | chr8:97156765-97156765 | 3'UTR | SNP | G | A | TCGA-BA-7269-01A-11D | ENST00000287020.5 | - | 0 | 1493 | TCGA | ||||
| tcga799 | RP11-145E5.5 | 0 | OT-TCGA | chr9 | 21974678 | 21974678 | g.chr9:21974678T>C | chr9:21974678-21974678 | Intron | SNP | T | C | rs587778189 | TCGA-BA-7269-01A-11D | ENST00000404796.2 | + | 5 | 460 | TCGA | |||
| tcga800 | GCNT1 | 2650 | OT-TCGA | chr9 | 79117750 | 79117750 | g.chr9:79117750C>T | chr9:79117750-79117750 | c.453C>T | c.(451-453)tgC>tgT | p.C151C | Silent | SNP | C | T | TCGA-BA-7269-01A-11D | ENST00000376730.4 | + | 4 | 936 | TCGA | |
| tcga801 | NOL8 | 55035 | OT-TCGA | chr9 | 95064013 | 95064013 | g.chr9:95064013C>G | chr9:95064013-95064013 | c.2881G>C | c.(2881-2883)Gaa>Caa | p.E961Q | Missense_Mutation | SNP | C | G | TCGA-BA-7269-01A-11D | ENST00000535387.1 | - | 11 | 2880 | TCGA | |
| tcga802 | CSTF2 | 1478 | OT-TCGA | chrX | 100078983 | 100078983 | g.chrX:100078983G>A | chrX:100078983-100078983 | c.553G>A | c.(553-555)Gaa>Aaa | p.E185K | Missense_Mutation | SNP | G | A | TCGA-BA-7269-01A-11D | ENST00000372972.2 | + | 5 | 569 | TCGA | |
| tcga803 | DCAF12L1 | 139170 | OT-TCGA | chrX | 125685719 | 125685719 | g.chrX:125685719G>A | chrX:125685719-125685719 | c.873C>T | c.(871-873)gcC>gcT | p.A291A | Silent | SNP | G | A | TCGA-BA-7269-01A-11D | ENST00000371126.1 | - | 1 | 1115 | TCGA | |
| tcga804 | ZNF185 | 7739 | OT-TCGA | chrX | 152113985 | 152113985 | g.chrX:152113985C>T | chrX:152113985-152113985 | c.1479C>T | c.(1477-1479)gtC>gtT | p.V493V | Silent | SNP | C | T | TCGA-BA-7269-01A-11D | ENST00000370270.2 | + | 17 | 1479 | TCGA | |
| tcga805 | DMD | 1756 | OT-TCGA | chrX | 31854842 | 31854842 | g.chrX:31854842G>T | chrX:31854842-31854842 | c.7193C>A | c.(7192-7194)cCa>cAa | p.P2398Q | Missense_Mutation | SNP | G | T | TCGA-BA-7269-01A-11D | ENST00000357033.4 | - | 49 | 7399 | TCGA | |
| tcga19072 | CTC-326K19.6(nearby) | 0 | OT-TCGA | chr19 | 50463939 | 50463939 | g.chr19:50463939G>A | chr19:50463939-50463939 | 5'Flank | SNP | G | A | TCGA-BA-7269-01A-11D | ENST00000451973.1 | - | 0 | 0 | TCGA | ||||
| tcga19073 | DNAH8(nearby) | 1769 | OT-TCGA | chr6 | 38690577 | 38690577 | g.chr6:38690577C>T | chr6:38690577-38690577 | 5'Flank | SNP | C | T | TCGA-BA-7269-01A-11D | ENST00000359357.3 | + | 0 | 0 | TCGA |