Search term NIBMG-F316-GB returned results from Exome Somatic dbGENVOC 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
esm9337 | NLRP14 | 338323 | OSCC_GB | chr11 | 7063625 | 7063625 | g.chr11:7063625G>T | chr11:7063625-7063625 | c.368G>T | c.(367-369)gGa>gTa | p.G123V | Missense_Mutation | SNP | G | T | - | NIBMG-F316-GB | ENST00000299481.4 | + | 4 | 714 | NIBMG |
esm9338 | PRDM4 | 11108 | OSCC_GB | chr12 | 108133235 | 108133235 | g.chr12:108133235T>G | chr12:108133235-108133235 | c.2018A>C | c.(2017-2019)aAt>aCt | p.N673T | Missense_Mutation | SNP | T | G | - | NIBMG-F316-GB | ENST00000228437.5 | - | 11 | 2477 | NIBMG |
esm9339 | ATP2A2 | 488 | OSCC_GB | chr12 | 110770416 | 110770416 | g.chr12:110770416C>T | chr12:110770416-110770416 | c.1110C>T | c.(1108-1110)gaC>gaT | p.D370D | Silent | SNP | C | T | - | NIBMG-F316-GB | ENST00000308664.6 | + | 9 | 1784 | NIBMG |
esm9340 | GSG1 | 83445 | OSCC_GB | chr12 | 13243490 | 13243490 | g.chr12:13243490C>T | chr12:13243490-13243490 | c.311G>A | c.(310-312)cGg>cAg | p.R104Q | Missense_Mutation | SNP | C | T | rs140139872 | NIBMG-F316-GB | ENST00000432710.2 | - | 2 | 443 | NIBMG |
esm9341 | USH2A | 7399 | OSCC_GB | chr1 | 215802301 | 215802301 | g.chr1:215802301C>T | chr1:215802301-215802301 | c.15374G>A | c.(15373-15375)cGc>cAc | p.R5125H | Missense_Mutation | SNP | C | T | rs189729452 | NIBMG-F316-GB | ENST00000307340.3 | - | 71 | 15760 | NIBMG |
esm9342 | PDE3A | 5139 | OSCC_GB | chr12 | 20769234 | 20769234 | g.chr12:20769234C>T | chr12:20769234-20769234 | c.1340C>T | c.(1339-1341)gCc>gTc | p.A447V | Missense_Mutation | SNP | C | T | - | NIBMG-F316-GB | ENST00000359062.3 | + | 4 | 1380 | NIBMG |
esm9343 | SCAF11 | 9169 | OSCC_GB | chr12 | 46345500 | 46345500 | g.chr12:46345500G>T | chr12:46345500-46345500 | c.230C>A | c.(229-231)tCa>tAa | p.S77* | Nonsense_Mutation | SNP | G | T | - | NIBMG-F316-GB | ENST00000369367.3 | - | 4 | 463 | NIBMG |
esm9344 | OR6C74 | 254783 | OSCC_GB | chr12 | 55641783 | 55641783 | g.chr12:55641783A>G | chr12:55641783-55641783 | c.712A>G | c.(712-714)Aca>Gca | p.T238A | Missense_Mutation | SNP | A | G | - | NIBMG-F316-GB | ENST00000343870.4 | + | 1 | 802 | NIBMG |
esm9345 | EIF5 | 1983 | OSCC_GB | chr14 | 103805613 | 103805613 | g.chr14:103805613T>A | chr14:103805613-103805613 | c.849T>A | c.(847-849)gtT>gtA | p.V283V | Silent | SNP | T | A | - | NIBMG-F316-GB | ENST00000216554.3 | + | 9 | 1525 | NIBMG |
esm9346 | ABHD4 | 63874 | OSCC_GB | chr14 | 23078649 | 23078649 | g.chr14:23078649G>T | chr14:23078649-23078649 | c.772G>T | c.(772-774)Gcc>Tcc | p.A258S | Missense_Mutation | SNP | G | T | - | NIBMG-F316-GB | ENST00000428304.2 | + | 6 | 842 | NIBMG |
esm9347 | SHC4 | 399694 | OSCC_GB | chr15 | 49135723 | 49135723 | g.chr15:49135723G>A | chr15:49135723-49135723 | c.1366C>T | c.(1366-1368)Cga>Tga | p.R456* | Nonsense_Mutation | SNP | G | A | - | NIBMG-F316-GB | ENST00000332408.4 | - | 10 | 1794 | NIBMG |
esm9348 | MROH7 | 374977 | OSCC_GB | chr1 | 55144987 | 55144987 | g.chr1:55144987G>A | chr1:55144987-55144987 | c.2101G>A | c.(2101-2103)Gcc>Acc | p.A701T | Missense_Mutation | SNP | G | A | rs554316180 | NIBMG-F316-GB | ENST00000421030.2 | + | 12 | 2386 | NIBMG |
esm9349 | GLCE | 26035 | OSCC_GB | chr15 | 69553539 | 69553539 | g.chr15:69553539G>A | chr15:69553539-69553539 | c.508G>A | c.(508-510)Gag>Aag | p.E170K | Missense_Mutation | SNP | G | A | - | NIBMG-F316-GB | ENST00000559420.2 | + | 2 | 713 | NIBMG |
esm9350 | CSPG4 | 1464 | OSCC_GB | chr15 | 75982111 | 75982111 | g.chr15:75982111A>T | chr15:75982111-75982111 | c.1295T>A | c.(1294-1296)cTg>cAg | p.L432Q | Missense_Mutation | SNP | A | T | - | NIBMG-F316-GB | ENST00000308508.5 | - | 3 | 1387 | NIBMG |
esm9351 | AKAP13 | 11214 | OSCC_GB | chr15 | 86262362 | 86262362 | g.chr15:86262362G>T | chr15:86262362-86262362 | c.6069G>T | c.(6067-6069)gtG>gtT | p.V2023V | Silent | SNP | G | T | - | NIBMG-F316-GB | ENST00000361243.2 | + | 23 | 6150 | NIBMG |
esm9352 | ACSM5 | 54988 | OSCC_GB | chr16 | 20435243 | 20435243 | g.chr16:20435243G>A | chr16:20435243-20435243 | c.773G>A | c.(772-774)tGg>tAg | p.W258* | Nonsense_Mutation | SNP | G | A | rs534281119 | NIBMG-F316-GB | ENST00000331849.4 | + | 6 | 920 | NIBMG |
esm9353 | AP1G1 | 164 | OSCC_GB | chr16 | 71783852 | 71783852 | g.chr16:71783852C>T | chr16:71783852-71783852 | c.1442G>A | c.(1441-1443)gGt>gAt | p.G481D | Missense_Mutation | SNP | C | T | - | NIBMG-F316-GB | ENST00000299980.4 | - | 15 | 1883 | NIBMG |
esm9354 | ATXN1L | 342371 | OSCC_GB | chr16 | 71883981 | 71883981 | g.chr16:71883981C>T | chr16:71883981-71883981 | c.338C>T | c.(337-339)gCg>gTg | p.A113V | Missense_Mutation | SNP | C | T | rs368965014 | NIBMG-F316-GB | ENST00000427980.2 | + | 3 | 631 | NIBMG |
esm9355 | LDHD | 197257 | OSCC_GB | chr16 | 75147961 | 75147961 | g.chr16:75147961C>A | chr16:75147961-75147961 | c.732G>T | c.(730-732)gaG>gaT | p.E244D | Missense_Mutation | SNP | C | A | rs141563074 | NIBMG-F316-GB | ENST00000450168.2 | - | 6 | 782 | NIBMG |
esm9356 | KLHL11 | 55175 | OSCC_GB | chr17 | 40010787 | 40010787 | g.chr17:40010787A>G | chr17:40010787-40010787 | c.1332T>C | c.(1330-1332)caT>caC | p.H444H | Silent | SNP | A | G | - | NIBMG-F316-GB | ENST00000319121.3 | - | 2 | 1392 | NIBMG |
esm9357 | AXIN2 | 8313 | OSCC_GB | chr17 | 63554671 | 63554671 | g.chr17:63554671C>T | chr17:63554671-63554671 | c.68G>A | c.(67-69)cGg>cAg | p.R23Q | Missense_Mutation | SNP | C | T | - | NIBMG-F316-GB | ENST00000375702.5 | - | 1 | 176 | NIBMG |
esm9358 | TP53 | 7157 | OSCC_GB | chr17 | 7578205 | 7578205 | g.chr17:7578205C>A | chr17:7578205-7578205 | c.644G>T | c.(643-645)aGt>aTt | p.S215I | Missense_Mutation | SNP | C | A | rs587782177 | NIBMG-F316-GB | ENST00000269305.4 | - | 6 | 833 | NIBMG |
esm9359 | MUC16 | 94025 | OSCC_GB | chr19 | 9083943 | 9083943 | g.chr19:9083943C>T | chr19:9083943-9083943 | c.7872G>A | c.(7870-7872)acG>acA | p.T2624T | Silent | SNP | C | T | - | NIBMG-F316-GB | ENST00000397910.4 | - | 1 | 8075 | NIBMG |
esm9360 | SLC24A3 | 57419 | OSCC_GB | chr20 | 19664867 | 19664867 | g.chr20:19664867T>C | chr20:19664867-19664867 | c.949T>C | c.(949-951)Tca>Cca | p.S317P | Missense_Mutation | SNP | T | C | - | NIBMG-F316-GB | ENST00000328041.6 | + | 11 | 1146 | NIBMG |
esm9361 | CHD6 | 84181 | OSCC_GB | chr20 | 40126088 | 40126088 | g.chr20:40126088C>T | chr20:40126088-40126088 | c.1028G>A | c.(1027-1029)cGc>cAc | p.R343H | Missense_Mutation | SNP | C | T | - | NIBMG-F316-GB | ENST00000373233.3 | - | 8 | 1205 | NIBMG |
esm9362 | CNTNAP5 | 129684 | OSCC_GB | chr2 | 125261995 | 125261995 | g.chr2:125261995C>T | chr2:125261995-125261995 | c.1186C>T | c.(1186-1188)Cga>Tga | p.R396* | Nonsense_Mutation | SNP | C | T | - | NIBMG-F316-GB | ENST00000431078.1 | + | 8 | 1550 | NIBMG |
esm9363 | PLCL1 | 5334 | OSCC_GB | chr2 | 198949862 | 198949862 | g.chr2:198949862G>T | chr2:198949862-198949862 | c.1621G>T | c.(1621-1623)Gga>Tga | p.G541* | Nonsense_Mutation | SNP | G | T | - | NIBMG-F316-GB | ENST00000428675.1 | + | 2 | 2019 | NIBMG |
esm9364 | CASP8 | 841 | OSCC_GB | chr2 | 202137484 | 202137484 | g.chr2:202137484G>A | chr2:202137484-202137484 | c.712G>A | c.(712-714)Gaa>Aaa | p.E238K | Missense_Mutation | SNP | G | A | - | NIBMG-F316-GB | ENST00000358485.4 | + | 4 | 908 | NIBMG |
esm9365 | PPP1CB | 5500 | OSCC_GB | chr2 | 29016749 | 29016749 | g.chr2:29016749A>T | chr2:29016749-29016749 | c.765A>T | c.(763-765)gaA>gaT | p.E255D | Missense_Mutation | SNP | A | T | - | NIBMG-F316-GB | ENST00000395366.2 | + | 7 | 1037 | NIBMG |
esm9366 | FAM179A | 165186 | OSCC_GB | chr2 | 29237382 | 29237382 | g.chr2:29237382C>T | chr2:29237382-29237382 | c.999C>T | c.(997-999)gcC>gcT | p.A333A | Silent | SNP | C | T | - | NIBMG-F316-GB | ENST00000379558.4 | + | 8 | 1350 | NIBMG |
esm9367 | PLCXD2 | 257068 | OSCC_GB | chr3 | 111427221 | 111427221 | g.chr3:111427221G>A | chr3:111427221-111427221 | c.612G>A | c.(610-612)gaG>gaA | p.E204E | Silent | SNP | G | A | - | NIBMG-F316-GB | ENST00000477665.1 | + | 2 | 936 | NIBMG |
esm9368 | STXBP5L | 9515 | OSCC_GB | chr3 | 121134709 | 121134709 | g.chr3:121134709G>T | chr3:121134709-121134709 | c.3192G>T | c.(3190-3192)atG>atT | p.M1064I | Missense_Mutation | SNP | G | T | rs13094925 | NIBMG-F316-GB | ENST00000273666.6 | + | 26 | 3463 | NIBMG |
esm9369 | ZMAT3 | 64393 | OSCC_GB | chr3 | 178745469 | 178745469 | g.chr3:178745469C>T | chr3:178745469-178745469 | c.522G>A | c.(520-522)agG>agA | p.R174R | Silent | SNP | C | T | - | NIBMG-F316-GB | ENST00000311417.2 | - | 4 | 1263 | NIBMG |
esm9370 | CADPS | 8618 | OSCC_GB | chr3 | 62388794 | 62388794 | g.chr3:62388794G>A | chr3:62388794-62388794 | c.3844C>T | c.(3844-3846)Cat>Tat | p.H1282Y | Missense_Mutation | SNP | G | A | - | NIBMG-F316-GB | ENST00000383710.4 | - | 29 | 4193 | NIBMG |
esm9371 | NFKB1 | 4790 | OSCC_GB | chr4 | 103531853 | 103531853 | g.chr4:103531853G>T | chr4:103531853-103531853 | c.2349G>T | c.(2347-2349)tgG>tgT | p.W783C | Missense_Mutation | SNP | G | T | - | NIBMG-F316-GB | ENST00000226574.4 | + | 20 | 2816 | NIBMG |
esm9372 | ZNF518B | 85460 | OSCC_GB | chr4 | 10445078 | 10445078 | g.chr4:10445078C>A | chr4:10445078-10445078 | c.2875G>T | c.(2875-2877)Gtg>Ttg | p.V959L | Missense_Mutation | SNP | C | A | - | NIBMG-F316-GB | ENST00000326756.3 | - | 3 | 3313 | NIBMG |
esm9373 | CLCN3 | 1182 | OSCC_GB | chr4 | 170628250 | 170628250 | g.chr4:170628250G>A | chr4:170628250-170628250 | c.1982G>A | c.(1981-1983)cGa>cAa | p.R661Q | Missense_Mutation | SNP | G | A | - | NIBMG-F316-GB | ENST00000347613.4 | + | 11 | 2536 | NIBMG |
esm9374 | TENM3 | 55714 | OSCC_GB | chr4 | 183675875 | 183675875 | g.chr4:183675875A>G | chr4:183675875-183675875 | c.4355A>G | c.(4354-4356)aAt>aGt | p.N1452S | Missense_Mutation | SNP | A | G | - | NIBMG-F316-GB | ENST00000511685.1 | + | 22 | 4478 | NIBMG |
esm9375 | NCOA7 | 135112 | OSCC_GB | chr6 | 126248880 | 126248880 | g.chr6:126248880C>T | chr6:126248880-126248880 | c.2595C>T | c.(2593-2595)ctC>ctT | p.L865L | Silent | SNP | C | T | - | NIBMG-F316-GB | ENST00000368357.3 | + | 15 | 2947 | NIBMG |
esm9376 | HIVEP2 | 3097 | OSCC_GB | chr6 | 143092736 | 143092736 | g.chr6:143092736C>T | chr6:143092736-143092736 | c.3140G>A | c.(3139-3141)cGg>cAg | p.R1047Q | Missense_Mutation | SNP | C | T | - | NIBMG-F316-GB | ENST00000367604.1 | - | 4 | 3779 | NIBMG |
esm9377 | RAET1L | 154064 | OSCC_GB | chr6 | 150342225 | 150342225 | g.chr6:150342225T>G | chr6:150342225-150342225 | c.447A>C | c.(445-447)ctA>ctC | p.L149L | Silent | SNP | T | G | rs532329436 | NIBMG-F316-GB | ENST00000367341.1 | - | 3 | 446 | NIBMG |
esm9378 | PRPF4B | 8899 | OSCC_GB | chr6 | 4044187 | 4044187 | g.chr6:4044187G>T | chr6:4044187-4044187 | c.1791G>T | c.(1789-1791)cgG>cgT | p.R597R | Silent | SNP | G | T | - | NIBMG-F316-GB | ENST00000337659.6 | + | 6 | 1891 | NIBMG |
esm9379 | KLHDC10 | 23008 | OSCC_GB | chr7 | 129760622 | 129760622 | g.chr7:129760622G>T | chr7:129760622-129760622 | c.509G>T | c.(508-510)gGa>gTa | p.G170V | Missense_Mutation | SNP | G | T | - | NIBMG-F316-GB | ENST00000335420.5 | + | 4 | 643 | NIBMG |
esm9380 | SNX10 | 29887 | OSCC_GB | chr7 | 26404668 | 26404668 | g.chr7:26404668C>A | chr7:26404668-26404668 | c.214C>A | c.(214-216)Caa>Aaa | p.Q72K | Splice_Site | SNP | C | A | - | NIBMG-F316-GB | ENST00000338523.4 | + | 5 | 401 | NIBMG |
esm9381 | SNTG1 | 54212 | OSCC_GB | chr8 | 51415411 | 51415411 | g.chr8:51415411T>A | chr8:51415411-51415411 | c.437T>A | c.(436-438)cTc>cAc | p.L146H | Missense_Mutation | SNP | T | A | - | NIBMG-F316-GB | ENST00000522124.1 | + | 9 | 1098 | NIBMG |
esm9382 | STX17 | 55014 | OSCC_GB | chr9 | 102713363 | 102713363 | g.chr9:102713363G>T | chr9:102713363-102713363 | c.211G>T | c.(211-213)Gaa>Taa | p.E71* | Nonsense_Mutation | SNP | G | T | - | NIBMG-F316-GB | ENST00000259400.6 | + | 4 | 347 | NIBMG |
esm9383 | PGM5 | 5239 | OSCC_GB | chr9 | 71094402 | 71094402 | g.chr9:71094402C>T | chr9:71094402-71094402 | c.1228C>T | c.(1228-1230)Cgg>Tgg | p.R410W | Missense_Mutation | SNP | C | T | - | NIBMG-F316-GB | ENST00000396396.1 | + | 8 | 1457 | NIBMG |
esm9384 | GABRA3 | 2556 | OSCC_GB | chrX | 151336984 | 151336984 | g.chrX:151336984C>T | chrX:151336984-151336984 | c.1195G>A | c.(1195-1197)Gtg>Atg | p.V399M | Missense_Mutation | SNP | C | T | - | NIBMG-F316-GB | ENST00000370314.4 | - | 10 | 1433 | NIBMG |
esm9385 | USP9X | 8239 | OSCC_GB | chrX | 41077699 | 41077699 | g.chrX:41077699A>G | chrX:41077699-41077699 | c.6284A>G | c.(6283-6285)aAt>aGt | p.N2095S | Missense_Mutation | SNP | A | G | - | NIBMG-F316-GB | ENST00000378308.2 | + | 37 | 6917 | NIBMG |
No records found for this search term NIBMG-F316-GB from TCGA data