Search term OT54 returned NO results from Exome Somatic dbGENVOC section.
No records found for this search term OT54 from TCGA data
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| esj971 | NLGN4X | 57502 | OTSCC | chrX | 5811555 | 5811555 | g.chrX:5811555G>A | chrX:5811555-5811555 | c.1754C>T | c.(1753-1755)aCg>aTg | p.T585M | Missense_Mutation | SNP | G | A | OT54 | ENST00000381095.3 | - | 6 | 2381 | 26834999 | |
| esj1000 | MAGEB1 | 4112 | OTSCC | chrX | 30269613 | 30269613 | g.chrX:30269613C>T | chrX:30269613-30269613 | c.1003C>T | c.(1003-1005)Cgt>Tgt | p.R335C | Missense_Mutation | SNP | C | T | OT54 | ENST00000378981.3 | + | 4 | 1324 | 26834999 | |
| esj1178 | ATAD3C | 219293 | OTSCC | chr1 | 1403973 | 1403974 | g.chr1:1403973_1403974insG | chr1:1403973-1403974 | 3'UTR | INS | - | G | OT54 | ENST00000378785.2 | + | 0 | 2294_2295 | 26834999 | ||||
| esj1298 | PADI1 | 29943 | OTSCC | chr1 | 17557178 | 17557178 | g.chr1:17557178C>T | chr1:17557178-17557178 | Intron | SNP | C | T | rs2977235 | OT54 | ENST00000375471.4 | + | 10 | 1253 | 26834999 | |||
| esj1339 | MAP3K6 | 9064 | OTSCC | chr1 | 27687466 | 27687466 | g.chr1:27687466G>T | chr1:27687466-27687466 | c.1866C>A | c.(1864-1866)aaC>aaA | p.N622K | Missense_Mutation | SNP | G | T | rs35659744 | OT54 | ENST00000493901.1 | - | 15 | 2105 | 26834999 |
| esj1613 | ADAM15 | 8751 | OTSCC | chr1 | 155029832 | 155029832 | g.chr1:155029832C>T | chr1:155029832-155029832 | c.1317C>T | c.(1315-1317)ttC>ttT | p.F439F | Silent | SNP | C | T | OT54 | ENST00000356955.2 | + | 12 | 1418 | 26834999 | |
| esj1693 | RNF2 | 6045 | OTSCC | chr1 | 185067515 | 185067515 | g.chr1:185067515A>C | chr1:185067515-185067515 | Intron | SNP | A | C | rs368038035 | OT54 | ENST00000367510.3 | + | 5 | 1025 | 26834999 | |||
| esj1801 | FMN2 | 56776 | OTSCC | chr1 | 240370932 | 240370932 | g.chr1:240370932G>A | chr1:240370932-240370932 | c.2820G>A | c.(2818-2820)gcG>gcA | p.A940A | Silent | SNP | G | A | rs145628188|rs71170718|rs562038978 | OT54 | ENST00000319653.9 | + | 5 | 3050 | 26834999 |
| esj1802 | FMN2 | 56776 | OTSCC | chr1 | 240370940 | 240370940 | g.chr1:240370940C>T | chr1:240370940-240370940 | c.2828C>T | c.(2827-2829)cCt>cTt | p.P943L | Missense_Mutation | SNP | C | T | rs199628038|rs71170718|rs562038978 | OT54 | ENST00000319653.9 | + | 5 | 3058 | 26834999 |
| esj1815 | ZNF670 | 93474 | OTSCC | chr1 | 247241850 | 247241850 | g.chr1:247241850G>C | chr1:247241850-247241850 | Intron | SNP | G | C | rs41305955 | OT54 | ENST00000366503.2 | - | 1 | 162 | 26834999 | |||
| esj1942 | RAB11FIP5 | 26056 | OTSCC | chr2 | 73339708 | 73339708 | g.chr2:73339708G>A | chr2:73339708-73339708 | c.198C>T | c.(196-198)tgC>tgT | p.C66C | Silent | SNP | G | A | rs1864488 | OT54 | ENST00000258098.6 | - | 1 | 438 | 26834999 |
| esj2024 | PSD4 | 23550 | OTSCC | chr2 | 113956371 | 113956371 | g.chr2:113956371G>C | chr2:113956371-113956371 | c.2592G>C | c.(2590-2592)acG>acC | p.T864T | Silent | SNP | G | C | rs2276561 | OT54 | ENST00000441564.3 | + | 15 | 2761 | 26834999 |
| esj2176 | AC079354.1 | 0 | OTSCC | chr2 | 202965204 | 202965205 | g.chr2:202965204_202965205delGA | chr2:202965204-202965205 | Intron | DEL | GA | - | rs150039982 | OT54 | ENST00000409515.3 | + | 7 | 1494 | 26834999 | |||
| esj2398 | ARHGEF3 | 50650 | OTSCC | chr3 | 56992904 | 56992904 | g.chr3:56992904G>C | chr3:56992904-56992904 | c.76C>G | c.(76-78)Cgg>Ggg | p.R26G | Missense_Mutation | SNP | G | C | OT54 | ENST00000338458.4 | - | 3 | 185 | 26834999 | |
| esj2664 | IDUA | 3425 | OTSCC | chr4 | 996165 | 996165 | g.chr4:996165G>A | chr4:996165-996165 | c.1081G>A | c.(1081-1083)Gcg>Acg | p.A361T | Missense_Mutation | SNP | G | A | rs6831280 | OT54 | ENST00000247933.4 | + | 8 | 1169 | 26834999 |
| esj2670 | RP11-503N18.1 | 0 | OTSCC | chr4 | 2429067 | 2429067 | g.chr4:2429067T>C | chr4:2429067-2429067 | ncRNA | SNP | T | C | rs6842928 | OT54 | ENST00000382849.2 | + | 0 | 885 | 26834999 | |||
| esj2708 | GBA3 | 57733 | OTSCC | chr4 | 22820673 | 22820674 | g.chr4:22820673_22820674insA | chr4:22820673-22820674 | ncRNA | INS | - | A | OT54 | ENST00000503442.1 | + | 0 | 707_708 | 26834999 | ||||
| esj2709 | GBA3 | 57733 | OTSCC | chr4 | 22820676 | 22820676 | g.chr4:22820676T>G | chr4:22820676-22820676 | ncRNA | SNP | T | G | rs5015834|rs200861082|rs371903826|rs5856716 | OT54 | ENST00000503442.1 | + | 0 | 710 | 26834999 | |||
| esj2717 | KLB | 152831 | OTSCC | chr4 | 39436055 | 39436055 | g.chr4:39436055G>A | chr4:39436055-39436055 | c.1051G>A | c.(1051-1053)Gtt>Att | p.V351I | Missense_Mutation | SNP | G | A | OT54 | ENST00000257408.4 | + | 2 | 1148 | 26834999 | |
| esj2819 | ANXA5 | 308 | OTSCC | chr4 | 122617718 | 122617718 | g.chr4:122617718G>C | chr4:122617718-122617718 | Intron | SNP | G | C | rs2306417 | OT54 | ENST00000296511.5 | - | 2 | 295 | 26834999 | |||
| esj2876 | AGA | 175 | OTSCC | chr4 | 178363378 | 178363378 | g.chr4:178363378G>A | chr4:178363378-178363378 | Intron | SNP | G | A | rs11131799 | OT54 | ENST00000264595.2 | - | 1 | 255 | 26834999 | |||
| esj2994 | ARSB | 411 | OTSCC | chr5 | 78111674 | 78111674 | g.chr5:78111674A>G | chr5:78111674-78111674 | Intron | SNP | A | G | rs34152768 | OT54 | ENST00000264914.4 | - | 6 | 1750 | 26834999 | |||
| esj3087 | FCHSD1 | 89848 | OTSCC | chr5 | 141023723 | 141023723 | g.chr5:141023723T>C | chr5:141023723-141023723 | Intron | SNP | T | C | rs468920 | OT54 | ENST00000522126.1 | - | 16 | 1832 | 26834999 | |||
| esj3234 | ZNRD1-AS1 | 80862 | OTSCC | chr6 | 29975192 | 29975196 | g.chr6:29975192_29975196delCATCG | chr6:29975192-29975196 | ncRNA | DEL | CATCG | - | rs386698684|rs200029204|rs201432109 | OT54 | ENST00000376797.3 | - | 0 | 1172 | 26834999 | |||
| esj3237 | ZNRD1-AS1 | 80862 | OTSCC | chr6 | 29975199 | 29975199 | g.chr6:29975199C>G | chr6:29975199-29975199 | ncRNA | SNP | C | G | rs386698684|rs200029204 | OT54 | ENST00000376797.3 | - | 0 | 1172 | 26834999 | |||
| esj3238 | ZNRD1-AS1 | 80862 | OTSCC | chr6 | 29975201 | 29975203 | g.chr6:29975201_29975203delGAA | chr6:29975201-29975203 | ncRNA | DEL | GAA | - | rs386698684|rs201045049|rs369789432 | OT54 | ENST00000376797.3 | - | 0 | 1172 | 26834999 | |||
| esj3264 | HLA-B | 3106 | OTSCC | chr6 | 31321803 | 31321803 | g.chr6:31321803G>A | chr6:31321803-31321803 | 3'UTR | SNP | G | A | rs3180225 | OT54 | ENST00000412585.2 | - | 0 | 1392 | 26834999 | |||
| esj3326 | HLA-DRB1 | 3123 | OTSCC | chr6 | 32546795 | 32546799 | g.chr6:32546795_32546799delTGCCA | chr6:32546795-32546799 | 3'UTR | DEL | TGCCA | - | rs71864678|rs1064701 | OT54 | ENST00000360004.5 | - | 0 | 975_979 | 26834999 | |||
| esj3439 | MRPL2 | 51069 | OTSCC | chr6 | 43021989 | 43021989 | g.chr6:43021989delC | chr6:43021989-43021989 | 3'UTR | DEL | C | - | rs554839691 | OT54 | ENST00000230413.5 | - | 0 | 879 | 26834999 | |||
| esj3600 | PDE10A | 10846 | OTSCC | chr6 | 165809946 | 165809946 | g.chr6:165809946C>T | chr6:165809946-165809946 | c.1281G>A | c.(1279-1281)atG>atA | p.M427I | Missense_Mutation | SNP | C | T | OT54 | ENST00000539869.2 | - | 14 | 1336 | 26834999 | |
| esj3765 | SRRM3 | 222183 | OTSCC | chr7 | 75915291 | 75915291 | g.chr7:75915291G>A | chr7:75915291-75915291 | 3'UTR | SNP | G | A | rs200253789 | OT54 | ENST00000326382.8 | + | 0 | 2299 | 26834999 | |||
| esj4012 | CSMD1 | 64478 | OTSCC | chr8 | 3165276 | 3165276 | g.chr8:3165276C>T | chr8:3165276-3165276 | c.3894G>A | c.(3892-3894)ccG>ccA | p.P1298P | Silent | SNP | C | T | rs191537593 | OT54 | ENST00000520002.1 | - | 26 | 4449 | 26834999 |
| esj4050 | SLC39A14 | 23516 | OTSCC | chr8 | 22262515 | 22262515 | g.chr8:22262515G>C | chr8:22262515-22262515 | Intron | SNP | G | C | rs549185508 | OT54 | ENST00000359741.5 | + | 2 | 445 | 26834999 | |||
| esj4104 | PREX2 | 80243 | OTSCC | chr8 | 69009335 | 69009335 | g.chr8:69009335G>T | chr8:69009335-69009335 | c.2452G>T | c.(2452-2454)Gaa>Taa | p.E818* | Nonsense_Mutation | SNP | G | T | OT54 | ENST00000288368.4 | + | 22 | 2729 | 26834999 | |
| esj4195 | PLEC | 5339 | OTSCC | chr8 | 145006127 | 145006127 | g.chr8:145006127delT | chr8:145006127-145006127 | c.2567delA | c.(2566-2568)aagfs | p.K856fs | Frame_Shift_Del | DEL | T | - | OT54 | ENST00000322810.4 | - | 18 | 2736 | 26834999 | |
| esj4285 | ANKRD20A1 | 84210 | OTSCC | chr9 | 67926873 | 67926873 | g.chr9:67926873A>G | chr9:67926873-67926873 | c.1A>G | c.(1-3)Atg>Gtg | p.M1V | Start_Codon_SNP | SNP | A | G | OT54 | ENST00000377477.2 | + | 1 | 113 | 26834999 | |
| esj4286 | ANKRD20A1 | 84210 | OTSCC | chr9 | 67926890 | 67926890 | g.chr9:67926890C>T | chr9:67926890-67926890 | c.18C>T | c.(16-18)ttC>ttT | p.F6F | Silent | SNP | C | T | OT54 | ENST00000377477.2 | + | 1 | 130 | 26834999 | |
| esj4287 | ANKRD20A1 | 84210 | OTSCC | chr9 | 67927043 | 67927043 | g.chr9:67927043C>T | chr9:67927043-67927043 | c.171C>T | c.(169-171)agC>agT | p.S57S | Silent | SNP | C | T | OT54 | ENST00000377477.2 | + | 1 | 283 | 26834999 | |
| esj4288 | ANKRD20A1 | 84210 | OTSCC | chr9 | 67927052 | 67927052 | g.chr9:67927052G>A | chr9:67927052-67927052 | c.180G>A | c.(178-180)ctG>ctA | p.L60L | Silent | SNP | G | A | OT54 | ENST00000377477.2 | + | 1 | 292 | 26834999 | |
| esj4587 | NRP1 | 8829 | OTSCC | chr10 | 33491507 | 33491515 | g.chr10:33491507_33491515delTGAAAATAA | chr10:33491507-33491515 | Intron | DEL | TGAAAATAA | - | rs139666910 | OT54 | ENST00000265371.4 | - | 12 | 2390 | 26834999 | |||
| esj4601 | RET | 5979 | OTSCC | chr10 | 43600689 | 43600689 | g.chr10:43600689A>G | chr10:43600689-43600689 | Intron | SNP | A | G | rs2435352 | OT54 | ENST00000355710.3 | + | 4 | 1099 | 26834999 | |||
| esj4636 | FAM21A | 387680 | OTSCC | chr10 | 51827839 | 51827839 | g.chr10:51827839T>C | chr10:51827839-51827839 | Intron | SNP | T | C | rs113882441 | OT54 | ENST00000282633.5 | + | 2 | 48 | 26834999 | |||
| esj4981 | MTCH2 | 23788 | OTSCC | chr11 | 47663951 | 47663951 | g.chr11:47663951A>G | chr11:47663951-47663951 | c.67T>C | c.(67-69)Tac>Cac | p.Y23H | Missense_Mutation | SNP | A | G | rs200816454 | OT54 | ENST00000302503.3 | - | 1 | 224 | 26834999 |
| esj4982 | MTCH2 | 23788 | OTSCC | chr11 | 47663958 | 47663958 | g.chr11:47663958C>T | chr11:47663958-47663958 | c.60G>A | c.(58-60)ccG>ccA | p.P20P | Silent | SNP | C | T | OT54 | ENST00000302503.3 | - | 1 | 217 | 26834999 | |
| esj4983 | MTCH2 | 23788 | OTSCC | chr11 | 47663959 | 47663959 | g.chr11:47663959G>C | chr11:47663959-47663959 | c.59C>G | c.(58-60)cCg>cGg | p.P20R | Missense_Mutation | SNP | G | C | rs201627714 | OT54 | ENST00000302503.3 | - | 1 | 216 | 26834999 |
| esj4984 | MTCH2 | 23788 | OTSCC | chr11 | 47663963 | 47663963 | g.chr11:47663963G>A | chr11:47663963-47663963 | c.55C>T | c.(55-57)Cag>Tag | p.Q19* | Nonsense_Mutation | SNP | G | A | rs76185606 | OT54 | ENST00000302503.3 | - | 1 | 212 | 26834999 |
| esj4985 | MTCH2 | 23788 | OTSCC | chr11 | 47663986 | 47663986 | g.chr11:47663986C>T | chr11:47663986-47663986 | c.32G>A | c.(31-33)gGc>gAc | p.G11D | Missense_Mutation | SNP | C | T | rs72909898 | OT54 | ENST00000302503.3 | - | 1 | 189 | 26834999 |
| esj4986 | MTCH2 | 23788 | OTSCC | chr11 | 47663996 | 47663996 | g.chr11:47663996C>T | chr11:47663996-47663996 | c.22G>A | c.(22-24)Gtg>Atg | p.V8M | Missense_Mutation | SNP | C | T | rs72909899 | OT54 | ENST00000302503.3 | - | 1 | 179 | 26834999 |
| esj5031 | HNRNPUL2 | 221092 | OTSCC | chr11 | 62488918 | 62488918 | g.chr11:62488918A>G | chr11:62488918-62488918 | Intron | SNP | A | G | rs77694397 | OT54 | ENST00000301785.5 | - | 9 | 1675 | 26834999 | |||
| esj5150 | RAB39A | 54734 | OTSCC | chr11 | 107832683 | 107832683 | g.chr11:107832683G>A | chr11:107832683-107832683 | c.239G>A | c.(238-240)cGa>cAa | p.R80Q | Missense_Mutation | SNP | G | A | OT54 | ENST00000320578.2 | + | 2 | 305 | 26834999 | |
| esj5189 | SORL1 | 6653 | OTSCC | chr11 | 121437638 | 121437639 | g.chr11:121437638_121437639insCTTCCCTCCAGGAAGCAATGCCTGGGCACACAGGCATTG | chr11:121437638-121437639 | Intron | INS | - | CTTCCCTCCAGGAAGCAATGCCTGGGCACACAGGCATTG | OT54 | ENST00000260197.7 | + | 22 | 3178 | 26834999 | ||||
| esj5369 | POU6F1 | 5463 | OTSCC | chr12 | 51590638 | 51590638 | g.chr12:51590638C>T | chr12:51590638-51590638 | 5'UTR | SNP | C | T | rs151163072 | OT54 | ENST00000389243.4 | - | 0 | 928 | 26834999 | |||
| esj5382 | KRT1 | 3848 | OTSCC | chr12 | 53069229 | 53069229 | g.chr12:53069229G>A | chr12:53069229-53069229 | c.1683C>T | c.(1681-1683)tcC>tcT | p.S561S | Silent | SNP | G | A | rs540699806|rs267607656 | OT54 | ENST00000252244.3 | - | 9 | 1741 | 26834999 |
| esj5384 | KRT1 | 3848 | OTSCC | chr12 | 53069243 | 53069243 | g.chr12:53069243T>C | chr12:53069243-53069243 | c.1669A>G | c.(1669-1671)Agc>Ggc | p.S557G | Missense_Mutation | SNP | T | C | rs77846840|rs540699806|rs267607656 | OT54 | ENST00000252244.3 | - | 9 | 1727 | 26834999 |
| esj5442 | TRHDE | 29953 | OTSCC | chr12 | 73057088 | 73057088 | g.chr12:73057088G>A | chr12:73057088-73057088 | 3'UTR | SNP | G | A | rs73146999 | OT54 | ENST00000261180.4 | + | 0 | 3284 | 26834999 | |||
| esj5498 | MYO1H | 283446 | OTSCC | chr12 | 109835550 | 109835550 | g.chr12:109835550C>T | chr12:109835550-109835550 | c.455C>T | c.(454-456)gCc>gTc | p.A152V | Missense_Mutation | SNP | C | T | OT54 | ENST00000310903.5 | + | 5 | 561 | 26834999 | |
| esj5547 | MLXIP | 22877 | OTSCC | chr12 | 122517071 | 122517072 | g.chr12:122517071_122517072insACAGACGTGCCAGACCT | chr12:122517071-122517072 | c.312_313insACAGACGTGCCAGACCT | c.(313-315)cagfs | p.Q105fs | Frame_Shift_Ins | INS | - | ACAGACGTGCCAGACCT | OT54 | ENST00000319080.7 | + | 1 | 444_445 | 26834999 | |
| esj5579 | RIMBP2 | 23504 | OTSCC | chr12 | 130897142 | 130897142 | g.chr12:130897142T>C | chr12:130897142-130897142 | Intron | SNP | T | C | OT54 | ENST00000261655.4 | - | 15 | 2985 | 26834999 | ||||
| esj5609 | ATP12A | 479 | OTSCC | chr13 | 25281398 | 25281398 | g.chr13:25281398G>A | chr13:25281398-25281398 | Intron | SNP | G | A | rs565148736 | OT54 | ENST00000381946.3 | + | 17 | 2505 | 26834999 | |||
| esj5758 | TGM1 | 7051 | OTSCC | chr14 | 24718401 | 24718401 | g.chr14:24718401C>T | chr14:24718401-24718401 | 3'UTR | SNP | C | T | rs531264904|rs144344499|rs41294726|rs2748536 | OT54 | ENST00000206765.6 | - | 0 | 2695 | 26834999 | |||
| esj5806 | LRRC9 | 341883 | OTSCC | chr14 | 60441269 | 60441269 | g.chr14:60441269C>G | chr14:60441269-60441269 | Intron | SNP | C | G | OT54 | ENST00000445360.1 | + | 13 | 1710 | 26834999 | ||||
| esj5918 | C14orf79 | 122616 | OTSCC | chr14 | 105457771 | 105457771 | g.chr14:105457771A>G | chr14:105457771-105457771 | Intron | SNP | A | G | rs2247140 | OT54 | ENST00000547315.1 | + | 3 | 1208 | 26834999 | |||
| esj6002 | U8 | 0 | OTSCC | chr15 | 30936941 | 30936941 | g.chr15:30936941G>T | chr15:30936941-30936941 | ncRNA | SNP | G | T | rs138514498|rs67309432|rs35282460 | OT54 | ENST00000516793.1 | + | 0 | 128 | 26834999 | |||
| esj6007 | CHRNA7 | 1139 | OTSCC | chr15 | 32323030 | 32323030 | g.chr15:32323030C>G | chr15:32323030-32323030 | Intron | SNP | C | G | rs544887619 | OT54 | ENST00000454250.3 | + | 2 | 249 | 26834999 | |||
| esj6061 | CTD-2008A1.2 | 0 | OTSCC | chr15 | 45123756 | 45123757 | g.chr15:45123756_45123757insC | chr15:45123756-45123757 | ncRNA | INS | - | C | OT54 | ENST00000561384.2 | - | 0 | 870_871 | 26834999 | ||||
| esj6162 | NTRK3 | 4916 | OTSCC | chr15 | 88576185 | 88576185 | g.chr15:88576185G>C | chr15:88576185-88576185 | c.1194C>G | c.(1192-1194)gcC>gcG | p.A398A | Silent | SNP | G | C | rs2229910 | OT54 | ENST00000542733.2 | - | 12 | 1353 | 26834999 |
| esj6287 | PKD1 | 5310 | OTSCC | chr16 | 2161213 | 2161213 | g.chr16:2161213C>T | chr16:2161213-2161213 | c.3955G>A | c.(3955-3957)Ggg>Agg | p.G1319R | Missense_Mutation | SNP | C | T | OT54 | ENST00000262304.4 | - | 15 | 4163 | 26834999 | |
| esj6333 | GRIN2A | 2903 | OTSCC | chr16 | 9856870 | 9856872 | g.chr16:9856870_9856872delCAA | chr16:9856870-9856872 | 3'UTR | DEL | CAA | - | rs146199312 | OT54 | ENST00000396573.2 | - | 0 | 4838_4840 | 26834999 | |||
| esj6536 | ADAMTS18 | 170692 | OTSCC | chr16 | 77389816 | 77389816 | g.chr16:77389816C>A | chr16:77389816-77389816 | Intron | SNP | C | A | OT54 | ENST00000282849.5 | - | 9 | 1879 | 26834999 | ||||
| esj6675 | TP53 | 7157 | OTSCC | chr17 | 7579391 | 7579391 | g.chr17:7579391G>A | chr17:7579391-7579391 | c.296C>T | c.(295-297)tCc>tTc | p.S99F | Missense_Mutation | SNP | G | A | OT54 | ENST00000269305.4 | - | 4 | 485 | 26834999 | |
| esj6877 | HOXB13 | 10481 | OTSCC | chr17 | 46805397 | 46805397 | g.chr17:46805397C>A | chr17:46805397-46805397 | c.559G>T | c.(559-561)Gaa>Taa | p.E187* | Nonsense_Mutation | SNP | C | A | OT54 | ENST00000290295.7 | - | 1 | 1143 | 26834999 | |
| esj6894 | C17orf67 | 339210 | OTSCC | chr17 | 54872439 | 54872439 | g.chr17:54872439T>C | chr17:54872439-54872439 | c.259A>G | c.(259-261)Att>Gtt | p.I87V | Missense_Mutation | SNP | T | C | rs72837329 | OT54 | ENST00000397861.2 | - | 7 | 1538 | 26834999 |
| esj6933 | ABCA9 | 10350 | OTSCC | chr17 | 66982498 | 66982498 | g.chr17:66982498C>T | chr17:66982498-66982498 | Intron | SNP | C | T | OT54 | ENST00000340001.4 | - | 32 | 4259 | 26834999 | ||||
| esj6976 | C1QTNF1 | 114897 | OTSCC | chr17 | 77044219 | 77044220 | g.chr17:77044219_77044220insGCTGACCCCAGGGCTCAGCACCAG | chr17:77044219-77044220 | 3'UTR | INS | - | GCTGACCCCAGGGCTCAGCACCAG | OT54 | ENST00000311661.4 | + | 0 | 974_975 | 26834999 | ||||
| esj6992 | CHMP6 | 79643 | OTSCC | chr17 | 78972228 | 78972228 | g.chr17:78972228C>T | chr17:78972228-78972228 | Intron | SNP | C | T | OT54 | ENST00000325167.5 | + | 7 | 628 | 26834999 | ||||
| esj7041 | RP11-815J4.6 | 0 | OTSCC | chr18 | 12076471 | 12076471 | g.chr18:12076471G>A | chr18:12076471-12076471 | ncRNA | SNP | G | A | OT54 | ENST00000591780.1 | - | 0 | 124 | 26834999 | ||||
| esj7267 | PPAN-P2RY11 | 692312 | OTSCC | chr19 | 10221086 | 10221086 | g.chr19:10221086C>T | chr19:10221086-10221086 | Intron | SNP | C | T | rs74668408 | OT54 | ENST00000428358.1 | + | 9 | 1073 | 26834999 | |||
| esj7307 | EMR2 | 30817 | OTSCC | chr19 | 14887596 | 14887596 | g.chr19:14887596A>G | chr19:14887596-14887596 | 5'UTR | SNP | A | G | rs2286362 | OT54 | ENST00000315576.3 | - | 0 | 424 | 26834999 | |||
| esj7397 | SLC7A10 | 56301 | OTSCC | chr19 | 33701478 | 33701478 | g.chr19:33701478C>T | chr19:33701478-33701478 | c.1158G>A | c.(1156-1158)acG>acA | p.T386T | Silent | SNP | C | T | rs150600610 | OT54 | ENST00000253188.4 | - | 9 | 1304 | 26834999 |
| esj7435 | LGALS7 | 3963 | OTSCC | chr19 | 39262681 | 39262681 | g.chr19:39262681A>G | chr19:39262681-39262681 | Intron | SNP | A | G | rs201209491 | OT54 | ENST00000378626.4 | - | 3 | 95 | 26834999 | |||
| esj7446 | MED29 | 55588 | OTSCC | chr19 | 39888449 | 39888449 | g.chr19:39888449C>T | chr19:39888449-39888449 | 3'UTR | SNP | C | T | rs519575 | OT54 | ENST00000315588.5 | + | 0 | 825 | 26834999 | |||
| esj7526 | LIG1 | 3978 | OTSCC | chr19 | 48626604 | 48626604 | g.chr19:48626604G>A | chr19:48626604-48626604 | Intron | SNP | G | A | rs3731007 | OT54 | ENST00000263274.7 | - | 22 | 2424 | 26834999 | |||
| esj8357 | ANXA5 | 308 | OTSCC | chr4 | 122617688 | 122617688 | g.chr4:122617688T>C | chr4:122617688-122617688 | Intron | SNP | T | C | rs2306416 | OT54 | ENST00000296511.5 | - | 2 | 295 | 26834999 | |||
| esj8405 | KIFC1 | 3833 | OTSCC | chr6 | 33377484 | 33377484 | g.chr6:33377484G>C | chr6:33377484-33377484 | 3'UTR | SNP | G | C | rs58223929|rs57440415|rs437874 | OT54 | ENST00000428849.2 | + | 0 | 2489 | 26834999 | |||
| esj8479 | TAF5 | 6877 | OTSCC | chr10 | 105133369 | 105133370 | g.chr10:105133369_105133370delAT | chr10:105133369-105133370 | Intron | DEL | AT | - | rs376602897 | OT54 | ENST00000369839.3 | + | 2 | 820 | 26834999 | |||
| esj8555 | FSIP1 | 161835 | OTSCC | chr15 | 40062825 | 40062825 | g.chr15:40062825delC | chr15:40062825-40062825 | Intron | DEL | C | - | rs112959149|rs1565560 | OT54 | ENST00000350221.3 | - | 3 | 336 | 26834999 | |||
| esj8556 | ZFYVE19 | 84936 | OTSCC | chr15 | 41099900 | 41099901 | g.chr15:41099900_41099901insGGGGC | chr15:41099900-41099901 | Intron | INS | - | GGGGC | rs369585041 | OT54 | ENST00000564258.1 | + | 1 | 583 | 26834999 | |||
| esj8599 | GRIN2C | 2905 | OTSCC | chr17 | 72843923 | 72843923 | g.chr17:72843923G>A | chr17:72843923-72843923 | Intron | SNP | G | A | rs3744192 | OT54 | ENST00000293190.5 | - | 8 | 1918 | 26834999 | |||
| esj8605 | CHMP6 | 79643 | OTSCC | chr17 | 78971155 | 78971155 | g.chr17:78971155C>A | chr17:78971155-78971155 | Intron | SNP | C | A | rs386799834|rs199925280 | OT54 | ENST00000325167.5 | + | 6 | 573 | 26834999 | |||
| esj8669 | BAGE2 | 85319 | OTSCC | chr21 | 11098684 | 11098684 | g.chr21:11098684A>G | chr21:11098684-11098684 | ncRNA | SNP | A | G | rs375907107 | OT54 | ENST00000470054.1 | - | 0 | 223 | 26834999 | |||
| esj8680 | SHANK3 | 85358 | OTSCC | chr22 | 51117766 | 51117766 | g.chr22:51117766T>C | chr22:51117766-51117766 | c.795T>C | c.(793-795)caT>caC | p.H265H | Silent | SNP | T | C | rs73172298 | OT54 | ENST00000414786.2 | + | 7 | 1022 | 26834999 |
| esj8681 | SHANK3 | 85358 | OTSCC | chr22 | 51117787 | 51117787 | g.chr22:51117787T>C | chr22:51117787-51117787 | c.816T>C | c.(814-816)taT>taC | p.Y272Y | Silent | SNP | T | C | rs73172299 | OT54 | ENST00000414786.2 | + | 7 | 1043 | 26834999 |
| esj8682 | SHANK3 | 85358 | OTSCC | chr22 | 51117800 | 51117800 | g.chr22:51117800G>A | chr22:51117800-51117800 | c.829G>A | c.(829-831)Ggg>Agg | p.G277R | Missense_Mutation | SNP | G | A | OT54 | ENST00000414786.2 | + | 7 | 1056 | 26834999 | |
| esj8683 | SHANK3 | 85358 | OTSCC | chr22 | 51117802 | 51117802 | g.chr22:51117802G>T | chr22:51117802-51117802 | c.831G>T | c.(829-831)ggG>ggT | p.G277G | Silent | SNP | G | T | rs199640422 | OT54 | ENST00000414786.2 | + | 7 | 1058 | 26834999 |
| esj8713 | WDR17 | 116966 | OTSCC | chr4 | 177100890 | 177100891 | g.chr4:177100890_177100891delAT | chr4:177100890-177100891 | 3'UTR | DEL | AT | - | rs148615406 | OT54 | ENST00000508596.1 | + | 0 | 4264_4265 | 26834999 | |||
| esj8747 | KRT1 | 3848 | OTSCC | chr12 | 53069235 | 53069235 | g.chr12:53069235G>A | chr12:53069235-53069235 | c.1677C>T | c.(1675-1677)taC>taT | p.Y559Y | Silent | SNP | G | A | rs540699806|rs11170232|rs267607656 | OT54 | ENST00000252244.3 | - | 9 | 1735 | 26834999 |
| esj8783 | SHANK3 | 85358 | OTSCC | chr22 | 51117811 | 51117811 | g.chr22:51117811C>T | chr22:51117811-51117811 | c.840C>T | c.(838-840)aaC>aaT | p.N280N | Silent | SNP | C | T | rs200400333 | OT54 | ENST00000414786.2 | + | 7 | 1067 | 26834999 |
| esj8801 | BCLAF1 | 9774 | OTSCC | chr6 | 136582615 | 136582620 | g.chr6:136582615_136582620delGCTACA | chr6:136582615-136582620 | c.2545delTGTAGC | c.(2545-2547)tgt>gt | p.C849del | Splice_Site | DEL | GCTACA | - | rs140096922|rs74741384 | OT54 | ENST00000531224.1 | - | 12 | 2797 | 26834999 |
| esj8818 | BAGE2 | 85319 | OTSCC | chr21 | 11098679 | 11098679 | g.chr21:11098679C>T | chr21:11098679-11098679 | ncRNA | SNP | C | T | rs115425198 | OT54 | ENST00000470054.1 | - | 0 | 223 | 26834999 | |||
| esj8824 | INPP5E | 56623 | OTSCC | chr9 | 139327600 | 139327601 | g.chr9:139327600_139327601insCGCCCACCCCTCCAGCCA | chr9:139327600-139327601 | Intron | INS | - | CGCCCACCCCTCCAGCCA | rs367840840 | OT54 | ENST00000371712.3 | - | 4 | 1562 | 26834999 | |||
| esj8831 | SIRPA | 140885 | OTSCC | chr20 | 1895964 | 1895965 | g.chr20:1895964_1895965delAC | chr20:1895964-1895965 | c.299_300delAC | c.(298-300)aacfs | p.N101fs | Frame_Shift_Del | DEL | AC | - | rs17855614|rs373583167|rs386811662 | OT54 | ENST00000358771.4 | + | 2 | 451_452 | 26834999 |
| esj8885 | CTBP1(nearby) | 1487 | OTSCC | chr4 | 1244267 | 1244267 | g.chr4:1244267A>G | chr4:1244267-1244267 | 5'Flank | SNP | A | G | rs2291199 | OT54 | ENST00000382952.3 | - | 0 | 0 | 26834999 | |||
| esj9031 | CLN3(nearby) | 1201 | OTSCC | chr16 | 28508447 | 28508447 | g.chr16:28508447A>G | chr16:28508447-28508447 | 5'Flank | SNP | A | G | rs40831 | OT54 | ENST00000569430.1 | - | 0 | 0 | 26834999 | |||
| esj9060 | CGB1(nearby) | 114335 | OTSCC | chr19 | 49542078 | 49542078 | g.chr19:49542078A>G | chr19:49542078-49542078 | 5'Flank | SNP | A | G | rs4002456 | OT54 | ENST00000301407.7 | - | 0 | 0 | 26834999 | |||
| esj9099 | PRSS1(nearby) | 5644 | OTSCC | chr7 | 142457317 | 142457318 | g.chr7:142457317_142457318insCAA | chr7:142457317-142457318 | 5'Flank | INS | - | CAA | OT54 | ENST00000311737.7 | + | 0 | 0 | 26834999 | ||||
| esj9639 | Unknown | 0 | OTSCC | chr12 | 9585631 | 9585631 | g.chr12:9585631C>T | chr12:9585631-9585631 | IGR | SNP | C | T | rs3874116 | OT54 | 26834999 | |||||||
| esj9890 | Unknown | 0 | OTSCC | chr2 | 91968881 | 91968881 | g.chr2:91968881C>T | chr2:91968881-91968881 | IGR | SNP | C | T | rs62144338 | OT54 | 26834999 | |||||||
| esj9945 | SH3BGRL3 | 83442 | OTSCC | chr1 | 26608843 | 26608843 | g.chr1:26608843C>A | chr1:26608843-26608843 | IGR | SNP | C | A | rs151149897|rs66614970|rs6667693 | OT54 | ENST00000270792.5 | + | 0 | 1655 | 26834999 | |||
| esj9970 | FRG2C | 100288801 | OTSCC | chr3 | 75718149 | 75718158 | g.chr3:75718149_75718158delGACTCGTTTG | chr3:75718149-75718158 | IGR | DEL | GACTCGTTTG | - | rs539304322|rs201490313 | OT54 | ENST00000464571.1 | + | 0 | 2075 | 26834999 | |||
| esj9975 | Unknown | 0 | OTSCC | chr11 | 48373834 | 48373834 | g.chr11:48373834delA | chr11:48373834-48373834 | IGR | DEL | A | - | rs75261463|rs144450763 | OT54 | 26834999 |