Mutation - TCGA |
Type | Chromosome | Start Position | End Position | Strand | Variant Classification | Variant Type | Reference Allele | Tumor_seq Allele 1 | Tumor_seq Allele 2 | Tumor Sample Barcode | Matched Norm Sample Barcode | Genome Change | cDNA Change | Codon Change | Protein Change |
BLCA | 4 | 6325128 | 6325128 | + | Missense_Mutation | SNP | G | G | C | TCGA-4Z-AA7M-01A-11D-A391-08 | TCGA-4Z-AA7M-10A-01D-A394-08 | g.chr4:6325128G>C | c.1245C>G | c.(1243-1245)atC>atG | p.I415M |
BLCA | 4 | 6325278 | 6325278 | + | Missense_Mutation | SNP | G | G | T | TCGA-BT-A20N-01A-11D-A14W-08 | TCGA-BT-A20N-11A-11D-A14W-08 | g.chr4:6325278G>T | c.1095C>A | c.(1093-1095)ttC>ttA | p.F365L |
BLCA | 4 | 6335373 | 6335373 | + | Silent | SNP | G | G | A | TCGA-BT-A20R-01A-12D-A16O-08 | TCGA-BT-A20R-11A-11D-A16O-08 | g.chr4:6335373G>A | c.876C>T | c.(874-876)agC>agT | p.S292S |
BLCA | 4 | 6335436 | 6335436 | + | Silent | SNP | G | G | A | TCGA-FD-A6TI-01A-11D-A32B-08 | TCGA-FD-A6TI-10A-01D-A329-08 | g.chr4:6335436G>A | c.813C>T | c.(811-813)ccC>ccT | p.P271P |
BLCA | 4 | 6349680 | 6349680 | + | Missense_Mutation | SNP | G | G | C | TCGA-DK-AA6S-01A-21D-A391-08 | TCGA-DK-AA6S-10A-01D-A394-08 | g.chr4:6349680G>C | c.683C>G | c.(682-684)tCt>tGt | p.S228C |
BLCA | 4 | 6380209 | 6380209 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-A6B1-01A-12D-A30E-08 | TCGA-DK-A6B1-10A-01D-A30H-08 | g.chr4:6380209C>T | c.259G>A | c.(259-261)Gag>Aag | p.E87K |
BLCA | 4 | 6473933 | 6473933 | + | Silent | SNP | C | C | T | TCGA-BT-A2LD-01A-12D-A20D-08 | TCGA-BT-A2LD-10A-01D-A20D-08 | g.chr4:6473933C>T | c.24G>A | c.(22-24)cgG>cgA | p.R8R |
BRCA | 4 | 6325179 | 6325179 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-A8-A06X-01A-21W-A019-09 | TCGA-A8-A06X-10A-01W-A021-09 | g.chr4:6325179delC | c.1194delG | c.(1192-1194)aagfs | p.K398fs |
CESC | 4 | 6325074 | 6325074 | + | Missense_Mutation | SNP | G | G | C | TCGA-EK-A2PL-01A-11D-A18J-09 | TCGA-EK-A2PL-10A-01D-A18J-09 | g.chr4:6325074G>C | c.1299C>G | c.(1297-1299)aaC>aaG | p.N433K |
CESC | 4 | 6331054 | 6331054 | + | Silent | SNP | G | G | C | TCGA-IR-A3LA-01A-11D-A22X-09 | TCGA-IR-A3LA-10A-01D-A22X-09 | g.chr4:6331054G>C | c.987C>G | c.(985-987)ctC>ctG | p.L329L |
CESC | 4 | 6374374 | 6374374 | + | Missense_Mutation | SNP | G | G | C | TCGA-MU-A51Y-01A-11D-A26G-09 | TCGA-MU-A51Y-10A-01D-A26G-09 | g.chr4:6374374G>C | c.501C>G | c.(499-501)atC>atG | p.I167M |
CESC | 4 | 6382809 | 6382809 | + | Missense_Mutation | SNP | G | G | C | TCGA-JW-A5VL-01A-11D-A28B-09 | TCGA-JW-A5VL-10A-01D-A28E-09 | g.chr4:6382809G>C | c.83C>G | c.(82-84)tCt>tGt | p.S28C |
COAD | 4 | 6325036 | 6325036 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-A01Q-01A-01W-A005-10 | TCGA-AA-A01Q-10A-01W-A005-10 | g.chr4:6325036A>G | c.1337T>C | c.(1336-1338)aTg>aCg | p.M446T |
COAD | 4 | 6325190 | 6325190 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3994-01A-01W-1073-09 | TCGA-AA-3994-10A-01W-1073-09 | g.chr4:6325190C>T | c.1183G>A | c.(1183-1185)Gtg>Atg | p.V395M |
COAD | 4 | 6325204 | 6325204 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3844-01A-01W-0995-10 | TCGA-AA-3844-10A-01W-0995-10 | g.chr4:6325204G>A | c.1169C>T | c.(1168-1170)cCa>cTa | p.P390L |
COAD | 4 | 6325234 | 6325234 | + | Missense_Mutation | SNP | T | T | C | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr4:6325234T>C | c.1139A>G | c.(1138-1140)gAa>gGa | p.E380G |
COAD | 4 | 6330987 | 6330987 | + | Splice_Site | SNP | A | A | G | TCGA-A6-6653-01A-11D-1771-10 | TCGA-A6-6653-10A-01D-1771-10 | g.chr4:6330987A>G | | c.e8+1 | |
COAD | 4 | 6330993 | 6330993 | + | Missense_Mutation | SNP | C | C | T | TCGA-F4-6856-01A-11D-1924-10 | TCGA-F4-6856-10A-01D-1924-10 | g.chr4:6330993C>T | c.1048G>A | c.(1048-1050)Gac>Aac | p.D350N |
COAD | 4 | 6331042 | 6331042 | + | Silent | SNP | G | G | A | TCGA-AA-3851-01A-01W-0995-10 | TCGA-AA-3851-10A-01W-0995-10 | g.chr4:6331042G>A | c.999C>T | c.(997-999)taC>taT | p.Y333Y |
COAD | 4 | 6335428 | 6335428 | + | Missense_Mutation | SNP | C | C | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr4:6335428C>T | c.821G>A | c.(820-822)cGc>cAc | p.R274H |
COAD | 4 | 6374292 | 6374292 | + | Missense_Mutation | SNP | G | G | A | TCGA-D5-5540-01A-01D-1650-10 | TCGA-D5-5540-10A-01D-1650-10 | g.chr4:6374292G>A | c.583C>T | c.(583-585)Cgc>Tgc | p.R195C |
COAD | 4 | 6374376 | 6374376 | + | Missense_Mutation | SNP | T | T | C | TCGA-CM-6675-01A-11D-1835-10 | TCGA-CM-6675-10A-01D-1835-10 | g.chr4:6374376T>C | c.499A>G | c.(499-501)Atc>Gtc | p.I167V |
COAD | 4 | 6374427 | 6374427 | + | Splice_Site | SNP | C | C | T | TCGA-D5-6540-01A-11D-1719-10 | TCGA-D5-6540-10A-01D-1719-10 | g.chr4:6374427C>T | c.448G>A | c.(448-450)Gtg>Atg | p.V150M |
COAD | 4 | 6377556 | 6377556 | + | Missense_Mutation | SNP | G | G | A | TCGA-F4-6459-01A-11D-1771-10 | TCGA-F4-6459-10A-01D-1771-10 | g.chr4:6377556G>A | c.437C>T | c.(436-438)aCg>aTg | p.T146M |
COAD | 4 | 6377557 | 6377557 | + | Missense_Mutation | SNP | T | T | C | TCGA-AD-5900-01A-11D-1650-10 | TCGA-AD-5900-10A-01D-1650-10 | g.chr4:6377557T>C | c.436A>G | c.(436-438)Acg>Gcg | p.T146A |
COAD | 4 | 6382805 | 6382805 | + | Silent | SNP | G | G | A | TCGA-A6-2672-01A-01W-0833-10 | TCGA-A6-2672-10A-01W-0833-10 | g.chr4:6382805G>A | c.87C>T | c.(85-87)acC>acT | p.T29T |
COADREAD | 4 | 6325036 | 6325036 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-A01Q-01A-01W-A005-10 | TCGA-AA-A01Q-10A-01W-A005-10 | g.chr4:6325036A>G | c.1337T>C | c.(1336-1338)aTg>aCg | p.M446T |
COADREAD | 4 | 6325190 | 6325190 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3994-01A-01W-1073-09 | TCGA-AA-3994-10A-01W-1073-09 | g.chr4:6325190C>T | c.1183G>A | c.(1183-1185)Gtg>Atg | p.V395M |
COADREAD | 4 | 6325204 | 6325204 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3844-01A-01W-0995-10 | TCGA-AA-3844-10A-01W-0995-10 | g.chr4:6325204G>A | c.1169C>T | c.(1168-1170)cCa>cTa | p.P390L |
COADREAD | 4 | 6325234 | 6325234 | + | Missense_Mutation | SNP | T | T | C | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr4:6325234T>C | c.1139A>G | c.(1138-1140)gAa>gGa | p.E380G |
COADREAD | 4 | 6330987 | 6330987 | + | Splice_Site | SNP | A | A | G | TCGA-A6-6653-01A-11D-1771-10 | TCGA-A6-6653-10A-01D-1771-10 | g.chr4:6330987A>G | | c.e8+1 | |
COADREAD | 4 | 6330993 | 6330993 | + | Missense_Mutation | SNP | C | C | T | TCGA-F4-6856-01A-11D-1924-10 | TCGA-F4-6856-10A-01D-1924-10 | g.chr4:6330993C>T | c.1048G>A | c.(1048-1050)Gac>Aac | p.D350N |
COADREAD | 4 | 6331012 | 6331012 | + | Silent | SNP | T | T | C | TCGA-AG-A026-01A-32W-A096-10 | TCGA-AG-A026-10A-01W-A096-10 | g.chr4:6331012T>C | c.1029A>G | c.(1027-1029)gaA>gaG | p.E343E |
COADREAD | 4 | 6331042 | 6331042 | + | Silent | SNP | G | G | A | TCGA-AA-3851-01A-01W-0995-10 | TCGA-AA-3851-10A-01W-0995-10 | g.chr4:6331042G>A | c.999C>T | c.(997-999)taC>taT | p.Y333Y |
COADREAD | 4 | 6335428 | 6335428 | + | Missense_Mutation | SNP | C | C | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr4:6335428C>T | c.821G>A | c.(820-822)cGc>cAc | p.R274H |
COADREAD | 4 | 6374292 | 6374292 | + | Missense_Mutation | SNP | G | G | A | TCGA-D5-5540-01A-01D-1650-10 | TCGA-D5-5540-10A-01D-1650-10 | g.chr4:6374292G>A | c.583C>T | c.(583-585)Cgc>Tgc | p.R195C |
COADREAD | 4 | 6374376 | 6374376 | + | Missense_Mutation | SNP | T | T | C | TCGA-CM-6675-01A-11D-1835-10 | TCGA-CM-6675-10A-01D-1835-10 | g.chr4:6374376T>C | c.499A>G | c.(499-501)Atc>Gtc | p.I167V |
COADREAD | 4 | 6374427 | 6374427 | + | Splice_Site | SNP | C | C | T | TCGA-D5-6540-01A-11D-1719-10 | TCGA-D5-6540-10A-01D-1719-10 | g.chr4:6374427C>T | c.448G>A | c.(448-450)Gtg>Atg | p.V150M |
COADREAD | 4 | 6377556 | 6377556 | + | Missense_Mutation | SNP | G | G | A | TCGA-F4-6459-01A-11D-1771-10 | TCGA-F4-6459-10A-01D-1771-10 | g.chr4:6377556G>A | c.437C>T | c.(436-438)aCg>aTg | p.T146M |
COADREAD | 4 | 6377557 | 6377557 | + | Missense_Mutation | SNP | T | T | C | TCGA-AD-5900-01A-11D-1650-10 | TCGA-AD-5900-10A-01D-1650-10 | g.chr4:6377557T>C | c.436A>G | c.(436-438)Acg>Gcg | p.T146A |
COADREAD | 4 | 6382753 | 6382753 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-3727-01A-01W-0899-10 | TCGA-AG-3727-10A-01W-0901-10 | g.chr4:6382753G>A | c.139C>T | c.(139-141)Cgg>Tgg | p.R47W |
COADREAD | 4 | 6382805 | 6382805 | + | Silent | SNP | G | G | A | TCGA-A6-2672-01A-01W-0833-10 | TCGA-A6-2672-10A-01W-0833-10 | g.chr4:6382805G>A | c.87C>T | c.(85-87)acC>acT | p.T29T |
DLBC | 4 | 6325285 | 6325285 | + | Missense_Mutation | SNP | C | C | T | TCGA-FF-A7CQ-01A-11D-A382-10 | TCGA-FF-A7CQ-10A-01D-A385-10 | g.chr4:6325285C>T | c.1088G>A | c.(1087-1089)cGc>cAc | p.R363H |
GBMLGG | 4 | 6325273 | 6325273 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-7010-01A-11D-2024-08 | TCGA-DU-7010-10A-01D-2024-08 | g.chr4:6325273C>T | c.1100G>A | c.(1099-1101)cGg>cAg | p.R367Q |
GBMLGG | 4 | 6380248 | 6380248 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-HT-7689-01A-11D-2253-08 | TCGA-HT-7689-10A-01D-2253-08 | g.chr4:6380248G>A | c.220C>T | c.(220-222)Cag>Tag | p.Q74* |
GBMLGG | 4 | 6473900 | 6473900 | + | Silent | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr4:6473900G>A | c.57C>T | c.(55-57)agC>agT | p.S19S |
GBMLGG | 4 | 6473947 | 6473947 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr4:6473947C>T | c.10G>A | c.(10-12)Gac>Aac | p.D4N |
HNSC | 4 | 6335418 | 6335418 | + | Missense_Mutation | SNP | G | G | C | TCGA-D6-A4ZB-01A-11D-A25D-08 | TCGA-D6-A4ZB-10A-01D-A25E-08 | g.chr4:6335418G>C | c.831C>G | c.(829-831)ttC>ttG | p.F277L |
HNSC | 4 | 6374335 | 6374335 | + | Silent | SNP | G | G | A | TCGA-CV-7568-01A-11D-2229-08 | TCGA-CV-7568-10A-01D-2229-08 | g.chr4:6374335G>A | c.540C>T | c.(538-540)tcC>tcT | p.S180S |
KIPAN | 4 | 6335365 | 6335365 | + | Missense_Mutation | SNP | T | T | C | TCGA-Q2-A5QZ-01A-11D-A28G-10 | TCGA-Q2-A5QZ-10A-01D-A28G-10 | g.chr4:6335365T>C | c.884A>G | c.(883-885)tAc>tGc | p.Y295C |
KIPAN | 4 | 6349697 | 6349697 | + | Silent | SNP | C | C | T | TCGA-B8-5545-01A-01D-1669-08 | TCGA-B8-5545-10A-01D-1669-08 | g.chr4:6349697C>T | c.666G>A | c.(664-666)acG>acA | p.T222T |
KIPAN | 4 | 6374376 | 6374376 | + | Missense_Mutation | SNP | T | T | C | TCGA-B0-4839-01A-01D-1373-10 | TCGA-B0-4839-11A-01D-1373-10 | g.chr4:6374376T>C | c.499A>G | c.(499-501)Atc>Gtc | p.I167V |
KIRC | 4 | 6349697 | 6349697 | + | Silent | SNP | C | C | T | TCGA-B8-5545-01A-01D-1669-08 | TCGA-B8-5545-10A-01D-1669-08 | g.chr4:6349697C>T | c.666G>A | c.(664-666)acG>acA | p.T222T |
KIRC | 4 | 6374376 | 6374376 | + | Missense_Mutation | SNP | T | T | C | TCGA-B0-4839-01A-01D-1373-10 | TCGA-B0-4839-11A-01D-1373-10 | g.chr4:6374376T>C | c.499A>G | c.(499-501)Atc>Gtc | p.I167V |
KIRP | 4 | 6335365 | 6335365 | + | Missense_Mutation | SNP | T | T | C | TCGA-Q2-A5QZ-01A-11D-A28G-10 | TCGA-Q2-A5QZ-10A-01D-A28G-10 | g.chr4:6335365T>C | c.884A>G | c.(883-885)tAc>tGc | p.Y295C |
LGG | 4 | 6325273 | 6325273 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-7010-01A-11D-2024-08 | TCGA-DU-7010-10A-01D-2024-08 | g.chr4:6325273C>T | c.1100G>A | c.(1099-1101)cGg>cAg | p.R367Q |
LGG | 4 | 6380248 | 6380248 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-HT-7689-01A-11D-2253-08 | TCGA-HT-7689-10A-01D-2253-08 | g.chr4:6380248G>A | c.220C>T | c.(220-222)Cag>Tag | p.Q74* |
LGG | 4 | 6473900 | 6473900 | + | Silent | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr4:6473900G>A | c.57C>T | c.(55-57)agC>agT | p.S19S |
LGG | 4 | 6473947 | 6473947 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr4:6473947C>T | c.10G>A | c.(10-12)Gac>Aac | p.D4N |
LIHC | 4 | 6335429 | 6335429 | + | Missense_Mutation | SNP | G | G | A | TCGA-DD-A1EJ-01A-11D-A152-10 | TCGA-DD-A1EJ-10A-01D-A152-10 | g.chr4:6335429G>A | c.820C>T | c.(820-822)Cgc>Tgc | p.R274C |
LIHC | 4 | 6377634 | 6377634 | + | Missense_Mutation | SNP | A | A | T | TCGA-CC-A3MB-01A-11D-A20W-10 | TCGA-CC-A3MB-10A-01D-A20W-10 | g.chr4:6377634A>T | c.359T>A | c.(358-360)aTt>aAt | p.I120N |
LUAD | 4 | 6325220 | 6325220 | + | Silent | SNP | G | G | T | TCGA-MN-A4N1-01A-11D-A24P-08 | TCGA-MN-A4N1-10A-01D-A24P-08 | g.chr4:6325220G>T | c.1153C>A | c.(1153-1155)Cgg>Agg | p.R385R |
LUAD | 4 | 6331042 | 6331042 | + | Silent | SNP | G | G | A | TCGA-97-A4M1-01A-11D-A24P-08 | TCGA-97-A4M1-10A-01D-A24P-08 | g.chr4:6331042G>A | c.999C>T | c.(997-999)taC>taT | p.Y333Y |
LUAD | 4 | 6335430 | 6335430 | + | Silent | SNP | G | G | A | TCGA-55-8301-01A-11D-2284-08 | TCGA-55-8301-10A-01D-2284-08 | g.chr4:6335430G>A | c.819C>T | c.(817-819)aaC>aaT | p.N273N |
LUAD | 4 | 6349667 | 6349667 | + | Silent | SNP | C | C | T | TCGA-05-4398-01A-01D-1265-08 | TCGA-05-4398-10A-01D-1265-08 | g.chr4:6349667C>T | c.696G>A | c.(694-696)ccG>ccA | p.P232P |
LUAD | 4 | 6377594 | 6377594 | + | Missense_Mutation | SNP | C | C | A | TCGA-55-8620-01A-11D-2393-08 | TCGA-55-8620-10A-01D-2393-08 | g.chr4:6377594C>A | c.399G>T | c.(397-399)aaG>aaT | p.K133N |
LUAD | 4 | 6377597 | 6377597 | + | Silent | SNP | C | C | T | TCGA-17-Z022-01A-01W-0746-08 | TCGA-17-Z022-11A-01W-0746-08 | g.chr4:6377597C>T | c.396G>A | c.(394-396)ctG>ctA | p.L132L |
LUAD | 4 | 6380181 | 6380181 | + | Missense_Mutation | SNP | T | T | A | TCGA-50-5930-01A-11D-1753-08 | TCGA-50-5930-11A-01D-1753-08 | g.chr4:6380181T>A | c.287A>T | c.(286-288)aAg>aTg | p.K96M |
LUAD | 4 | 6380191 | 6380191 | + | Missense_Mutation | SNP | T | T | A | TCGA-55-7995-01A-11D-2184-08 | TCGA-55-7995-10A-01D-2184-08 | g.chr4:6380191T>A | c.277A>T | c.(277-279)Aac>Tac | p.N93Y |
LUAD | 4 | 6380272 | 6380272 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-73-4675-01A-01D-1265-08 | TCGA-73-4675-11A-01D-1265-08 | g.chr4:6380272C>A | c.196G>T | c.(196-198)Gaa>Taa | p.E66* |
LUAD | 4 | 6383531 | 6383531 | + | Intron | SNP | C | C | A | TCGA-55-7815-01A-11D-2167-08 | TCGA-55-7815-10A-01D-2167-08 | g.chr4:6383531C>A | | | |
LUSC | 4 | 6325261 | 6325261 | + | Missense_Mutation | SNP | C | C | T | TCGA-21-1081-01A-01D-1521-08 | TCGA-21-1081-10B-01D-1521-08 | g.chr4:6325261C>T | c.1112G>A | c.(1111-1113)cGg>cAg | p.R371Q |
LUSC | 4 | 6374278 | 6374278 | + | Missense_Mutation | SNP | C | C | A | TCGA-66-2787-01A-01D-0983-08 | TCGA-66-2787-11A-01D-0983-08 | g.chr4:6374278C>A | c.597G>T | c.(595-597)tgG>tgT | p.W199C |
OV | 4 | 6374374 | 6374374 | + | Silent | SNP | G | G | T | TCGA-09-2045-01A-01W-0799-08 | TCGA-09-2045-11A-01W-0799-08 | g.chr4:6374374G>T | c.501C>A | c.(499-501)atC>atA | p.I167I |
OV | 4 | 6377561 | 6377561 | + | Silent | SNP | C | C | T | TCGA-09-1675-01B-01W-0633-09 | TCGA-09-1675-10A-01W-0633-09 | g.chr4:6377561C>T | c.432G>A | c.(430-432)acG>acA | p.T144T |
PAAD | 4 | 6380234 | 6380234 | + | Silent | SNP | C | C | T | TCGA-US-A779-01A-11D-A32N-08 | TCGA-US-A779-11A-11D-A32N-08 | g.chr4:6380234C>T | c.234G>A | c.(232-234)ccG>ccA | p.P78P |
PAAD | 4 | 6383543 | 6383543 | + | Intron | SNP | G | G | A | TCGA-IB-AAUR-01A-21D-A38G-08 | TCGA-IB-AAUR-10A-01D-A38J-08 | g.chr4:6383543G>A | | | |
PAAD | 4 | 6473911 | 6473911 | + | Missense_Mutation | SNP | G | G | A | TCGA-HZ-A77O-01A-11D-A33T-08 | TCGA-HZ-A77O-10A-01D-A33W-08 | g.chr4:6473911G>A | c.46C>T | c.(46-48)Cgg>Tgg | p.R16W |
PCPG | 4 | 6380190 | 6380190 | + | Missense_Mutation | SNP | T | T | C | TCGA-QT-A7U0-01A-11D-A35D-08 | TCGA-QT-A7U0-10A-01D-A35B-08 | g.chr4:6380190T>C | c.278A>G | c.(277-279)aAc>aGc | p.N93S |
PRAD | 4 | 6377648 | 6377648 | + | Missense_Mutation | SNP | G | G | C | TCGA-CH-5788-01A-11D-1576-08 | TCGA-CH-5788-10A-01D-1576-08 | g.chr4:6377648G>C | c.345C>G | c.(343-345)atC>atG | p.I115M |
READ | 4 | 6331012 | 6331012 | + | Silent | SNP | T | T | C | TCGA-AG-A026-01A-32W-A096-10 | TCGA-AG-A026-10A-01W-A096-10 | g.chr4:6331012T>C | c.1029A>G | c.(1027-1029)gaA>gaG | p.E343E |
READ | 4 | 6382753 | 6382753 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-3727-01A-01W-0899-10 | TCGA-AG-3727-10A-01W-0901-10 | g.chr4:6382753G>A | c.139C>T | c.(139-141)Cgg>Tgg | p.R47W |
SARC | 4 | 6374262 | 6374262 | + | Missense_Mutation | SNP | C | C | T | TCGA-WK-A8XO-01A-11D-A37C-09 | TCGA-WK-A8XO-10A-01D-A37F-09 | g.chr4:6374262C>T | c.613G>A | c.(613-615)Gac>Aac | p.D205N |
SKCM | 4 | 6325200 | 6325200 | + | Silent | SNP | C | C | T | TCGA-EE-A180-06A-11D-A21A-08 | TCGA-EE-A180-10B-01D-A21A-08 | g.chr4:6325200C>T | c.1173G>A | c.(1171-1173)cgG>cgA | p.R391R |
SKCM | 4 | 6325221 | 6325221 | + | Silent | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr4:6325221G>A | c.1152C>T | c.(1150-1152)ccC>ccT | p.P384P |
SKCM | 4 | 6325235 | 6325235 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3J5-06A-11D-A20D-08 | TCGA-EE-A3J5-10A-01D-A20D-08 | g.chr4:6325235C>T | c.1138G>A | c.(1138-1140)Gaa>Aaa | p.E380K |
SKCM | 4 | 6335388 | 6335388 | + | Silent | SNP | C | C | T | TCGA-D3-A5GO-06A-12D-A27K-08 | TCGA-D3-A5GO-10A-01D-A27N-08 | g.chr4:6335388C>T | c.861G>A | c.(859-861)gtG>gtA | p.V287V |
SKCM | 4 | 6349649 | 6349649 | + | Silent | SNP | G | G | A | TCGA-EE-A180-06A-11D-A21A-08 | TCGA-EE-A180-10B-01D-A21A-08 | g.chr4:6349649G>A | c.714C>T | c.(712-714)ttC>ttT | p.F238F |
SKCM | 4 | 6349705 | 6349705 | + | Missense_Mutation | SNP | C | C | T | TCGA-DA-A1HV-06A-21D-A196-08 | TCGA-DA-A1HV-10A-01D-A198-08 | g.chr4:6349705C>T | c.658G>A | c.(658-660)Gac>Aac | p.D220N |
SKCM | 4 | 6349713 | 6349713 | + | Missense_Mutation | SNP | T | T | C | TCGA-D3-A51G-06A-11D-A25O-08 | TCGA-D3-A51G-10A-01D-A25O-08 | g.chr4:6349713T>C | c.650A>G | c.(649-651)aAc>aGc | p.N217S |
SKCM | 4 | 6349733 | 6349733 | + | Silent | SNP | G | G | A | TCGA-EE-A2MC-06A-12D-A197-08 | TCGA-EE-A2MC-10A-01D-A199-08 | g.chr4:6349733G>A | c.630C>T | c.(628-630)atC>atT | p.I210I |
SKCM | 4 | 6374257 | 6374257 | + | Silent | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr4:6374257C>T | c.618G>A | c.(616-618)agG>agA | p.R206R |
SKCM | 4 | 6374336 | 6374336 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3JA-06A-11D-A20D-08 | TCGA-EE-A3JA-10A-01D-A20D-08 | g.chr4:6374336G>A | c.539C>T | c.(538-540)tCc>tTc | p.S180F |
SKCM | 4 | 6374377 | 6374377 | + | Silent | SNP | C | C | T | TCGA-EE-A2MJ-06A-11D-A197-08 | TCGA-EE-A2MJ-10A-01D-A199-08 | g.chr4:6374377C>T | c.498G>A | c.(496-498)agG>agA | p.R166R |
SKCM | 4 | 6374389 | 6374389 | + | Silent | SNP | C | C | T | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr4:6374389C>T | c.486G>A | c.(484-486)gtG>gtA | p.V162V |
SKCM | 4 | 6377611 | 6377611 | + | Missense_Mutation | SNP | C | C | T | TCGA-GF-A6C9-06A-11D-A30X-08 | TCGA-GF-A6C9-10A-01D-A30X-08 | g.chr4:6377611C>T | c.382G>A | c.(382-384)Gaa>Aaa | p.E128K |
SKCM | 4 | 6377625 | 6377625 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3AC-06A-11D-A196-08 | TCGA-EE-A3AC-10A-01D-A198-08 | g.chr4:6377625C>T | c.368G>A | c.(367-369)cGa>cAa | p.R123Q |
SKCM | 4 | 6380203 | 6380203 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr4:6380203C>T | c.265G>A | c.(265-267)Gag>Aag | p.E89K |
SKCM | 4 | 6380219 | 6380219 | + | Silent | SNP | G | G | A | TCGA-ER-A19N-06A-11D-A197-08 | TCGA-ER-A19N-10A-01D-A199-08 | g.chr4:6380219G>A | c.249C>T | c.(247-249)ctC>ctT | p.L83L |
SKCM | 4 | 6380249 | 6380249 | + | Silent | SNP | G | G | A | TCGA-EE-A2MC-06A-12D-A197-08 | TCGA-EE-A2MC-10A-01D-A199-08 | g.chr4:6380249G>A | c.219C>T | c.(217-219)ttC>ttT | p.F73F |
SKCM | 4 | 6473925 | 6473925 | + | Missense_Mutation | SNP | T | T | A | TCGA-EE-A2MD-06A-11D-A197-08 | TCGA-EE-A2MD-10A-01D-A199-08 | g.chr4:6473925T>A | c.32A>T | c.(31-33)aAc>aTc | p.N11I |
SKCM | 4 | 6473933 | 6473933 | + | Silent | SNP | C | C | T | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr4:6473933C>T | c.24G>A | c.(22-24)cgG>cgA | p.R8R |