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 | 6 | 161771157 | 161771157 | + | Missense_Mutation | SNP | T | T | G | TCGA-DK-A3WY-01A-11D-A22Z-08 | TCGA-DK-A3WY-10A-01D-A22Z-08 | g.chr6:161771157T>G | c.1372A>C | c.(1372-1374)Atg>Ctg | p.M458L |
BLCA | 6 | 161807842 | 161807842 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-XF-A9T5-01A-11D-A42E-08 | TCGA-XF-A9T5-10A-01D-A42H-08 | g.chr6:161807842G>T | c.1151C>A | c.(1150-1152)tCa>tAa | p.S384* |
BLCA | 6 | 162622255 | 162622255 | + | Missense_Mutation | SNP | C | C | A | TCGA-CU-A3YL-01A-11D-A22Z-08 | TCGA-CU-A3YL-10A-01D-A22Z-08 | g.chr6:162622255C>A | c.442G>T | c.(442-444)Gtg>Ttg | p.V148L |
BLCA | 6 | 162683621 | 162683621 | + | Silent | SNP | A | A | G | TCGA-XF-A9SY-01A-21D-A42E-08 | TCGA-XF-A9SY-10A-01D-A42H-08 | g.chr6:162683621A>G | c.348T>C | c.(346-348)tcT>tcC | p.S116S |
BLCA | 6 | 162864342 | 162864342 | + | Splice_Site | SNP | C | C | T | TCGA-GV-A3JV-01A-11D-A21Z-08 | TCGA-GV-A3JV-10B-01D-A21Z-08 | g.chr6:162864342C>T | c.171G>A | c.(169-171)caG>caA | p.Q57Q |
BRCA | 6 | 161781222 | 161781222 | + | Missense_Mutation | SNP | C | C | T | TCGA-B6-A0I9-01A-11W-A050-09 | TCGA-B6-A0I9-10A-01W-A055-09 | g.chr6:161781222C>T | c.1183G>A | c.(1183-1185)Gaa>Aaa | p.E395K |
BRCA | 6 | 161969928 | 161969928 | + | Missense_Mutation | SNP | C | C | G | TCGA-C8-A1HM-01A-12D-A135-09 | TCGA-C8-A1HM-10A-01D-A135-09 | g.chr6:161969928C>G | c.1041G>C | c.(1039-1041)caG>caC | p.Q347H |
BRCA | 6 | 161969946 | 161969946 | + | Silent | SNP | C | C | A | TCGA-EW-A2FV-01A-11D-A17D-09 | TCGA-EW-A2FV-10A-01D-A17D-09 | g.chr6:161969946C>A | c.1023G>T | c.(1021-1023)ctG>ctT | p.L341L |
BRCA | 6 | 161969999 | 161969999 | + | Missense_Mutation | SNP | C | C | A | TCGA-BH-A0DX-01A-11D-A10Y-09 | TCGA-BH-A0DX-10A-02D-A110-09 | g.chr6:161969999C>A | c.970G>T | c.(970-972)Gtc>Ttc | p.V324F |
BRCA | 6 | 162622175 | 162622175 | + | Silent | SNP | G | G | C | TCGA-A7-A5ZV-01A-11D-A28B-09 | TCGA-A7-A5ZV-10A-01D-A28E-09 | g.chr6:162622175G>C | c.522C>G | c.(520-522)ctC>ctG | p.L174L |
BRCA | 6 | 162622238 | 162622238 | + | Silent | SNP | G | G | T | TCGA-A8-A09Z-01A-11W-A019-09 | TCGA-A8-A09Z-10A-01W-A021-09 | g.chr6:162622238G>T | c.459C>A | c.(457-459)ccC>ccA | p.P153P |
CESC | 6 | 161969941 | 161969941 | + | Missense_Mutation | SNP | G | G | A | TCGA-C5-A1MF-01A-11D-A13W-08 | TCGA-C5-A1MF-10A-01D-A13W-08 | g.chr6:161969941G>A | c.1028C>T | c.(1027-1029)cCg>cTg | p.P343L |
CESC | 6 | 162683699 | 162683699 | + | Silent | SNP | G | G | A | TCGA-EA-A5O9-01A-11D-A28B-09 | TCGA-EA-A5O9-10A-01D-A28E-09 | g.chr6:162683699G>A | c.270C>T | c.(268-270)aaC>aaT | p.N90N |
CESC | 6 | 162864488 | 162864488 | + | Missense_Mutation | SNP | A | A | C | TCGA-EA-A1QT-01A-11D-A14W-08 | TCGA-EA-A1QT-10A-01D-A14W-08 | g.chr6:162864488A>C | c.25T>G | c.(25-27)Tcc>Gcc | p.S9A |
COAD | 6 | 161781122 | 161781122 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr6:161781122delT | c.1283delA | c.(1282-1284)aatfs | p.N428fs |
COAD | 6 | 161781147 | 161781147 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr6:161781147G>A | c.1258C>T | c.(1258-1260)Cgc>Tgc | p.R420C |
COAD | 6 | 161781185 | 161781185 | + | Missense_Mutation | SNP | G | G | C | TCGA-CM-6678-01A-11D-1835-10 | TCGA-CM-6678-10A-01D-1835-10 | g.chr6:161781185G>C | c.1220C>G | c.(1219-1221)tCc>tGc | p.S407C |
COAD | 6 | 161807881 | 161807881 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3518-01A-02W-0833-10 | TCGA-AA-3518-10A-01W-0833-10 | g.chr6:161807881G>A | c.1112C>T | c.(1111-1113)gCg>gTg | p.A371V |
COAD | 6 | 161969982 | 161969983 | + | Frame_Shift_Ins | INS | - | - | C | TCGA-F4-6856-01A-11D-1924-10 | TCGA-F4-6856-10A-01D-1924-10 | g.chr6:161969982_161969983insC | c.986_987insG | c.(985-987)ggcfs | p.G329fs |
COAD | 6 | 161990440 | 161990440 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr6:161990440G>A | c.880C>T | c.(880-882)Ccc>Tcc | p.P294S |
COAD | 6 | 162394374 | 162394374 | + | Missense_Mutation | SNP | T | T | G | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr6:162394374T>G | c.694A>C | c.(694-696)Aat>Cat | p.N232H |
COAD | 6 | 162394403 | 162394403 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chr6:162394403G>T | c.665C>A | c.(664-666)aCa>aAa | p.T222K |
COAD | 6 | 162475180 | 162475180 | + | Missense_Mutation | SNP | T | T | G | TCGA-AA-3851-01A-01W-0995-10 | TCGA-AA-3851-10A-01W-0995-10 | g.chr6:162475180T>G | c.561A>C | c.(559-561)ttA>ttC | p.L187F |
COAD | 6 | 162683629 | 162683629 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr6:162683629C>A | c.340G>T | c.(340-342)Gga>Tga | p.G114* |
COAD | 6 | 162683711 | 162683711 | + | Silent | SNP | G | G | A | TCGA-D5-6539-01A-11D-1719-10 | TCGA-D5-6539-10A-01D-1719-10 | g.chr6:162683711G>A | c.258C>T | c.(256-258)gaC>gaT | p.D86D |
COAD | 6 | 162864383 | 162864383 | + | Missense_Mutation | SNP | T | T | G | TCGA-AA-3710-01A-01W-0995-10 | TCGA-AA-3710-10A-01W-0995-10 | g.chr6:162864383T>G | c.130A>C | c.(130-132)Att>Ctt | p.I44L |
COAD | 6 | 162864402 | 162864402 | + | Silent | SNP | C | C | T | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chr6:162864402C>T | c.111G>A | c.(109-111)ccG>ccA | p.P37P |
COADREAD | 6 | 161781122 | 161781122 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr6:161781122delT | c.1283delA | c.(1282-1284)aatfs | p.N428fs |
COADREAD | 6 | 161781147 | 161781147 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr6:161781147G>A | c.1258C>T | c.(1258-1260)Cgc>Tgc | p.R420C |
COADREAD | 6 | 161781185 | 161781185 | + | Missense_Mutation | SNP | G | G | C | TCGA-CM-6678-01A-11D-1835-10 | TCGA-CM-6678-10A-01D-1835-10 | g.chr6:161781185G>C | c.1220C>G | c.(1219-1221)tCc>tGc | p.S407C |
COADREAD | 6 | 161807881 | 161807881 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3518-01A-02W-0833-10 | TCGA-AA-3518-10A-01W-0833-10 | g.chr6:161807881G>A | c.1112C>T | c.(1111-1113)gCg>gTg | p.A371V |
COADREAD | 6 | 161969982 | 161969983 | + | Frame_Shift_Ins | INS | - | - | C | TCGA-F4-6856-01A-11D-1924-10 | TCGA-F4-6856-10A-01D-1924-10 | g.chr6:161969982_161969983insC | c.986_987insG | c.(985-987)ggcfs | p.G329fs |
COADREAD | 6 | 161990401 | 161990401 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr6:161990401G>T | c.919C>A | c.(919-921)Ctg>Atg | p.L307M |
COADREAD | 6 | 161990435 | 161990435 | + | Missense_Mutation | SNP | G | G | T | TCGA-F5-6571-01A-12D-1826-10 | TCGA-F5-6571-10A-01D-1826-10 | g.chr6:161990435G>T | c.885C>A | c.(883-885)aaC>aaA | p.N295K |
COADREAD | 6 | 161990440 | 161990440 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr6:161990440G>A | c.880C>T | c.(880-882)Ccc>Tcc | p.P294S |
COADREAD | 6 | 162394374 | 162394374 | + | Missense_Mutation | SNP | T | T | G | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr6:162394374T>G | c.694A>C | c.(694-696)Aat>Cat | p.N232H |
COADREAD | 6 | 162394403 | 162394403 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chr6:162394403G>T | c.665C>A | c.(664-666)aCa>aAa | p.T222K |
COADREAD | 6 | 162475138 | 162475138 | + | Silent | SNP | G | G | A | TCGA-AG-3892-01A-01W-1073-09 | TCGA-AG-3892-10A-01W-1073-09 | g.chr6:162475138G>A | c.603C>T | c.(601-603)tgC>tgT | p.C201C |
COADREAD | 6 | 162475180 | 162475180 | + | Missense_Mutation | SNP | T | T | G | TCGA-AA-3851-01A-01W-0995-10 | TCGA-AA-3851-10A-01W-0995-10 | g.chr6:162475180T>G | c.561A>C | c.(559-561)ttA>ttC | p.L187F |
COADREAD | 6 | 162683629 | 162683629 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr6:162683629C>A | c.340G>T | c.(340-342)Gga>Tga | p.G114* |
COADREAD | 6 | 162683711 | 162683711 | + | Silent | SNP | G | G | A | TCGA-D5-6539-01A-11D-1719-10 | TCGA-D5-6539-10A-01D-1719-10 | g.chr6:162683711G>A | c.258C>T | c.(256-258)gaC>gaT | p.D86D |
COADREAD | 6 | 162864376 | 162864376 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A00Y-01A-02W-A005-10 | TCGA-AG-A00Y-10A-01W-A005-10 | g.chr6:162864376G>T | c.137C>A | c.(136-138)gCa>gAa | p.A46E |
COADREAD | 6 | 162864383 | 162864383 | + | Missense_Mutation | SNP | T | T | G | TCGA-AA-3710-01A-01W-0995-10 | TCGA-AA-3710-10A-01W-0995-10 | g.chr6:162864383T>G | c.130A>C | c.(130-132)Att>Ctt | p.I44L |
COADREAD | 6 | 162864402 | 162864402 | + | Silent | SNP | C | C | T | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chr6:162864402C>T | c.111G>A | c.(109-111)ccG>ccA | p.P37P |
DLBC | 6 | 162206824 | 162206824 | + | Missense_Mutation | SNP | C | C | G | TCGA-FF-A7CR-01A-11D-A382-10 | TCGA-FF-A7CR-10A-01D-A385-10 | g.chr6:162206824C>G | c.851G>C | c.(850-852)gGc>gCc | p.G284A |
DLBC | 6 | 162475167 | 162475167 | + | Missense_Mutation | SNP | T | T | G | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr6:162475167T>G | c.574A>C | c.(574-576)Atg>Ctg | p.M192L |
DLBC | 6 | 162864492 | 162864492 | + | Missense_Mutation | SNP | G | G | C | TCGA-GR-7353-01A-11D-2210-10 | TCGA-GR-7353-10A-01D-2210-10 | g.chr6:162864492G>C | c.21C>G | c.(19-21)ttC>ttG | p.F7L |
ESCA | 6 | 161771153 | 161771153 | + | Missense_Mutation | SNP | C | C | T | TCGA-R6-A8W5-01B-11D-A37C-09 | TCGA-R6-A8W5-10A-01D-A37F-09 | g.chr6:161771153C>T | c.1376G>A | c.(1375-1377)gGg>gAg | p.G459E |
ESCA | 6 | 161969885 | 161969885 | + | Splice_Site | SNP | C | C | T | TCGA-L7-A6VZ-01A-12D-A33E-09 | TCGA-L7-A6VZ-10A-01D-A33H-09 | g.chr6:161969885C>T | | c.e9+1 | |
ESCA | 6 | 161990396 | 161990396 | + | Silent | SNP | T | T | C | TCGA-L5-A4OP-01A-11D-A27G-09 | TCGA-L5-A4OP-11A-11D-A27G-09 | g.chr6:161990396T>C | c.924A>G | c.(922-924)ggA>ggG | p.G308G |
ESCA | 6 | 162683700 | 162683700 | + | Missense_Mutation | SNP | T | T | G | TCGA-2H-A9GR-01A-12D-A37C-09 | TCGA-2H-A9GR-11A-11D-A37F-09 | g.chr6:162683700T>G | c.269A>C | c.(268-270)aAc>aCc | p.N90T |
GBM | 6 | 161771139 | 161771139 | + | Missense_Mutation | SNP | C | C | T | TCGA-06-6699-01A-11D-1845-08 | TCGA-06-6699-10A-01D-1845-08 | g.chr6:161771139C>T | c.1390G>A | c.(1390-1392)Gac>Aac | p.D464N |
GBMLGG | 6 | 161771139 | 161771139 | + | Missense_Mutation | SNP | C | C | T | TCGA-06-6699-01A-11D-1845-08 | TCGA-06-6699-10A-01D-1845-08 | g.chr6:161771139C>T | c.1390G>A | c.(1390-1392)Gac>Aac | p.D464N |
GBMLGG | 6 | 161781238 | 161781238 | + | Splice_Site | SNP | C | C | T | TCGA-HT-8012-01A-11D-2395-08 | TCGA-HT-8012-10A-01D-2396-08 | g.chr6:161781238C>T | | c.e11-1 | |
HNSC | 6 | 161771199 | 161771199 | + | Missense_Mutation | SNP | C | C | G | TCGA-D6-A6EK-01A-11D-A31L-08 | TCGA-D6-A6EK-10A-01D-A31J-08 | g.chr6:161771199C>G | c.1330G>C | c.(1330-1332)Gag>Cag | p.E444Q |
HNSC | 6 | 162683677 | 162683677 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-CN-6021-01A-11D-1683-08 | TCGA-CN-6021-10A-01D-1683-08 | g.chr6:162683677C>A | c.292G>T | c.(292-294)Gag>Tag | p.E98* |
HNSC | 6 | 162683695 | 162683695 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-CN-4727-01A-01D-1434-08 | TCGA-CN-4727-10A-01D-1434-08 | g.chr6:162683695delC | c.274delG | c.(274-276)gcgfs | p.A92fs |
HNSC | 6 | 162683729 | 162683729 | + | Missense_Mutation | SNP | C | C | A | TCGA-CN-6021-01A-11D-1683-08 | TCGA-CN-6021-10A-01D-1683-08 | g.chr6:162683729C>A | c.240G>T | c.(238-240)atG>atT | p.M80I |
KICH | 6 | 162206903 | 162206903 | + | Missense_Mutation | SNP | C | C | T | TCGA-KN-8428-01A-11D-2310-10 | TCGA-KN-8428-11A-01D-2311-10 | g.chr6:162206903C>T | c.772G>A | c.(772-774)Gtg>Atg | p.V258M |
KICH | 6 | 162394348 | 162394348 | + | Silent | SNP | C | C | A | TCGA-KL-8342-01A-11D-2310-10 | TCGA-KL-8342-11A-01D-2310-10 | g.chr6:162394348C>A | c.720G>T | c.(718-720)acG>acT | p.T240T |
KIPAN | 6 | 161781136 | 161781136 | + | Silent | SNP | T | T | C | TCGA-B0-5697-01A-11D-1534-10 | TCGA-B0-5697-11A-01D-1534-10 | g.chr6:161781136T>C | c.1269A>G | c.(1267-1269)gtA>gtG | p.V423V |
KIPAN | 6 | 162206852 | 162206852 | + | Missense_Mutation | SNP | G | G | C | TCGA-A4-8312-01A-11D-2396-08 | TCGA-A4-8312-10A-01D-2396-08 | g.chr6:162206852G>C | c.823C>G | c.(823-825)Cgg>Ggg | p.R275G |
KIPAN | 6 | 162206903 | 162206903 | + | Missense_Mutation | SNP | C | C | T | TCGA-KN-8428-01A-11D-2310-10 | TCGA-KN-8428-11A-01D-2311-10 | g.chr6:162206903C>T | c.772G>A | c.(772-774)Gtg>Atg | p.V258M |
KIPAN | 6 | 162394348 | 162394348 | + | Silent | SNP | C | C | A | TCGA-KL-8342-01A-11D-2310-10 | TCGA-KL-8342-11A-01D-2310-10 | g.chr6:162394348C>A | c.720G>T | c.(718-720)acG>acT | p.T240T |
KIPAN | 6 | 162864397 | 162864398 | + | Missense_Mutation | DNP | TC | TC | AT | TCGA-P4-AAVM-01A-11D-A42J-10 | TCGA-P4-AAVM-11A-11D-A42M-10 | g.chr6:162864397_162864398TC>AT | c.115_116GA>AT | c.(115-117)GAc>ATc | p.D39I |
KIRC | 6 | 161781136 | 161781136 | + | Silent | SNP | T | T | C | TCGA-B0-5697-01A-11D-1534-10 | TCGA-B0-5697-11A-01D-1534-10 | g.chr6:161781136T>C | c.1269A>G | c.(1267-1269)gtA>gtG | p.V423V |
KIRP | 6 | 162206852 | 162206852 | + | Missense_Mutation | SNP | G | G | C | TCGA-A4-8312-01A-11D-2396-08 | TCGA-A4-8312-10A-01D-2396-08 | g.chr6:162206852G>C | c.823C>G | c.(823-825)Cgg>Ggg | p.R275G |
KIRP | 6 | 162864397 | 162864398 | + | Missense_Mutation | DNP | TC | TC | AT | TCGA-P4-AAVM-01A-11D-A42J-10 | TCGA-P4-AAVM-11A-11D-A42M-10 | g.chr6:162864397_162864398TC>AT | c.115_116GA>AT | c.(115-117)GAc>ATc | p.D39I |
LGG | 6 | 161781238 | 161781238 | + | Splice_Site | SNP | C | C | T | TCGA-HT-8012-01A-11D-2395-08 | TCGA-HT-8012-10A-01D-2396-08 | g.chr6:161781238C>T | | c.e11-1 | |
LIHC | 6 | 162206857 | 162206857 | + | Missense_Mutation | SNP | T | T | C | TCGA-DD-A73A-01A-12D-A32G-10 | TCGA-DD-A73A-10A-01D-A32G-10 | g.chr6:162206857T>C | c.818A>G | c.(817-819)aAt>aGt | p.N273S |
LUAD | 6 | 161771171 | 161771171 | + | Missense_Mutation | SNP | C | C | A | TCGA-05-4390-01A-02D-1753-08 | TCGA-05-4390-10A-01D-1753-08 | g.chr6:161771171C>A | c.1358G>T | c.(1357-1359)tGg>tTg | p.W453L |
LUAD | 6 | 161781119 | 161781119 | + | Splice_Site | SNP | C | C | A | TCGA-49-4501-01A-01D-1265-08 | TCGA-49-4501-11A-01D-1265-08 | g.chr6:161781119C>A | | c.e11+1 | |
LUAD | 6 | 161781149 | 161781149 | + | Missense_Mutation | SNP | G | G | A | TCGA-44-8117-01A-11D-2238-08 | TCGA-44-8117-10A-01D-2238-08 | g.chr6:161781149G>A | c.1256C>T | c.(1255-1257)cCc>cTc | p.P419L |
LUAD | 6 | 161969900 | 161969900 | + | Missense_Mutation | SNP | C | C | A | TCGA-17-Z062-01A-01W-0747-08 | TCGA-17-Z062-11A-01W-0747-08 | g.chr6:161969900C>A | c.1069G>T | c.(1069-1071)Ggc>Tgc | p.G357C |
LUAD | 6 | 161969904 | 161969904 | + | Silent | SNP | G | G | T | TCGA-91-6848-01A-11D-1945-08 | TCGA-91-6848-11A-01D-1945-08 | g.chr6:161969904G>T | c.1065C>A | c.(1063-1065)ggC>ggA | p.G355G |
LUAD | 6 | 161969909 | 161969909 | + | Missense_Mutation | SNP | C | C | G | TCGA-05-4410-01A-21D-1855-08 | TCGA-05-4410-10A-01D-1855-08 | g.chr6:161969909C>G | c.1060G>C | c.(1060-1062)Ggg>Cgg | p.G354R |
LUAD | 6 | 161969912 | 161969912 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-55-7907-01A-11D-2167-08 | TCGA-55-7907-10A-01D-2167-08 | g.chr6:161969912C>A | c.1057G>T | c.(1057-1059)Gaa>Taa | p.E353* |
LUAD | 6 | 161969941 | 161969941 | + | Missense_Mutation | SNP | G | G | T | TCGA-64-5775-01A-01D-1625-08 | TCGA-64-5775-10A-01D-1625-08 | g.chr6:161969941G>T | c.1028C>A | c.(1027-1029)cCg>cAg | p.P343Q |
LUAD | 6 | 161970003 | 161970003 | + | Missense_Mutation | SNP | C | C | A | TCGA-55-A490-01A-11D-A24D-08 | TCGA-55-A490-10A-01D-A24F-08 | g.chr6:161970003C>A | c.966G>T | c.(964-966)gaG>gaT | p.E322D |
LUAD | 6 | 161970005 | 161970005 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-78-7155-01A-11D-2036-08 | TCGA-78-7155-10A-01D-2036-08 | g.chr6:161970005C>A | c.964G>T | c.(964-966)Gag>Tag | p.E322* |
LUAD | 6 | 162206851 | 162206851 | + | Missense_Mutation | SNP | C | C | G | TCGA-44-7670-01A-11D-2063-08 | TCGA-44-7670-10A-01D-2063-08 | g.chr6:162206851C>G | c.824G>C | c.(823-825)cGg>cCg | p.R275P |
LUAD | 6 | 162206908 | 162206908 | + | Missense_Mutation | SNP | C | C | T | TCGA-55-8097-01A-11D-2238-08 | TCGA-55-8097-10A-01D-2238-08 | g.chr6:162206908C>T | c.767G>A | c.(766-768)cGc>cAc | p.R256H |
LUAD | 6 | 162206910 | 162206910 | + | Silent | SNP | G | G | A | TCGA-95-7567-01A-11D-2063-08 | TCGA-95-7567-10A-01D-2063-08 | g.chr6:162206910G>A | c.765C>T | c.(763-765)tcC>tcT | p.S255S |
LUAD | 6 | 162206937 | 162206937 | + | Missense_Mutation | SNP | G | G | T | TCGA-55-8514-01A-11D-2393-08 | TCGA-55-8514-10A-01D-2393-08 | g.chr6:162206937G>T | c.738C>A | c.(736-738)agC>agA | p.S246R |
LUAD | 6 | 162394430 | 162394430 | + | Missense_Mutation | SNP | C | C | A | TCGA-05-4410-01A-21D-1855-08 | TCGA-05-4410-10A-01D-1855-08 | g.chr6:162394430C>A | c.638G>T | c.(637-639)gGa>gTa | p.G213V |
LUAD | 6 | 162475170 | 162475170 | + | Silent | SNP | G | G | T | TCGA-05-4424-01A-22D-1855-08 | TCGA-05-4424-10A-01D-1855-08 | g.chr6:162475170G>T | c.571C>A | c.(571-573)Cgg>Agg | p.R191R |
LUAD | 6 | 162622223 | 162622223 | + | Missense_Mutation | SNP | C | C | A | TCGA-99-8032-01A-11D-2238-08 | TCGA-99-8032-10A-01D-2238-08 | g.chr6:162622223C>A | c.474G>T | c.(472-474)caG>caT | p.Q158H |
LUAD | 6 | 162683557 | 162683557 | + | Splice_Site | SNP | C | C | G | TCGA-78-7159-01A-11D-2036-08 | TCGA-78-7159-10A-01D-2036-08 | g.chr6:162683557C>G | c.412G>C | c.(412-414)Gca>Cca | p.A138P |
LUAD | 6 | 162683597 | 162683597 | + | Silent | SNP | G | G | A | TCGA-55-8507-01A-11D-2393-08 | TCGA-55-8507-10A-01D-2393-08 | g.chr6:162683597G>A | c.372C>T | c.(370-372)caC>caT | p.H124H |
LUAD | 6 | 162683678 | 162683678 | + | Silent | SNP | C | C | A | TCGA-97-7554-01A-11D-2036-08 | TCGA-97-7554-10A-01D-2036-08 | g.chr6:162683678C>A | c.291G>T | c.(289-291)cgG>cgT | p.R97R |
LUAD | 6 | 162683714 | 162683714 | + | Silent | SNP | G | G | T | TCGA-86-A4JF-01A-11D-A24P-08 | TCGA-86-A4JF-10A-01D-A24P-08 | g.chr6:162683714G>T | c.255C>A | c.(253-255)ggC>ggA | p.G85G |
LUSC | 6 | 161781192 | 161781192 | + | Missense_Mutation | SNP | C | C | G | TCGA-66-2763-01A-01D-1522-08 | TCGA-66-2763-11A-01D-1522-08 | g.chr6:161781192C>G | c.1213G>C | c.(1213-1215)Gca>Cca | p.A405P |
LUSC | 6 | 161969928 | 161969928 | + | Missense_Mutation | SNP | C | C | A | TCGA-66-2757-01A-01D-1522-08 | TCGA-66-2757-11A-01D-1522-08 | g.chr6:161969928C>A | c.1041G>T | c.(1039-1041)caG>caT | p.Q347H |
LUSC | 6 | 161969933 | 161969933 | + | Missense_Mutation | SNP | C | C | T | TCGA-22-4593-01A-21D-1817-08 | TCGA-22-4593-11A-01D-1817-08 | g.chr6:161969933C>T | c.1036G>A | c.(1036-1038)Gac>Aac | p.D346N |
LUSC | 6 | 161990405 | 161990405 | + | Silent | SNP | C | C | T | TCGA-18-3409-01A-01D-0983-08 | TCGA-18-3409-11A-01D-0983-08 | g.chr6:161990405C>T | c.915G>A | c.(913-915)agG>agA | p.R305R |
LUSC | 6 | 161990421 | 161990421 | + | Missense_Mutation | SNP | T | T | C | TCGA-66-2754-01A-01D-0983-08 | TCGA-66-2754-11A-01D-0983-08 | g.chr6:161990421T>C | c.899A>G | c.(898-900)gAg>gGg | p.E300G |
LUSC | 6 | 162394383 | 162394383 | + | Missense_Mutation | SNP | T | T | A | TCGA-60-2713-01A-01D-1522-08 | TCGA-60-2713-11A-01D-1522-08 | g.chr6:162394383T>A | c.685A>T | c.(685-687)Atc>Ttc | p.I229F |
LUSC | 6 | 162394435 | 162394435 | + | Missense_Mutation | SNP | T | T | G | TCGA-21-5787-01A-01D-1632-08 | TCGA-21-5787-10A-01D-1632-08 | g.chr6:162394435T>G | c.633A>C | c.(631-633)aaA>aaC | p.K211N |
LUSC | 6 | 162475142 | 162475142 | + | Missense_Mutation | SNP | T | T | G | TCGA-21-1081-01A-01D-1521-08 | TCGA-21-1081-10B-01D-1521-08 | g.chr6:162475142T>G | c.599A>C | c.(598-600)cAc>cCc | p.H200P |
LUSC | 6 | 162475185 | 162475185 | + | Missense_Mutation | SNP | C | C | T | TCGA-34-2608-01A-02D-1522-08 | TCGA-34-2608-11A-01D-1522-08 | g.chr6:162475185C>T | c.556G>A | c.(556-558)Gtt>Att | p.V186I |
LUSC | 6 | 162683555 | 162683555 | + | Splice_Site | SNP | A | A | T | TCGA-66-2777-01A-01D-1267-08 | TCGA-66-2777-11A-01D-1267-08 | g.chr6:162683555A>T | | c.e3+1 | |
LUSC | 6 | 162683632 | 162683632 | + | Missense_Mutation | SNP | G | G | A | TCGA-18-3409-01A-01D-0983-08 | TCGA-18-3409-11A-01D-0983-08 | g.chr6:162683632G>A | c.337C>T | c.(337-339)Cca>Tca | p.P113S |
PAAD | 6 | 162394349 | 162394349 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr6:162394349G>A | c.719C>T | c.(718-720)aCg>aTg | p.T240M |
PAAD | 6 | 162622162 | 162622162 | + | Splice_Site | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr6:162622162C>T | | c.e4+1 | |
PAAD | 6 | 162864492 | 162864492 | + | Missense_Mutation | SNP | G | G | T | TCGA-IB-7652-01A-11D-2154-08 | TCGA-IB-7652-10A-01D-2154-08 | g.chr6:162864492G>T | c.21C>A | c.(19-21)ttC>ttA | p.F7L |
PRAD | 6 | 161969991 | 161969991 | + | Missense_Mutation | SNP | C | C | A | TCGA-CH-5754-01A-11D-1576-08 | TCGA-CH-5754-10A-01D-1576-08 | g.chr6:161969991C>A | c.978G>T | c.(976-978)caG>caT | p.Q326H |
PRAD | 6 | 162622177 | 162622177 | + | Missense_Mutation | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr6:162622177G>A | c.520C>T | c.(520-522)Ctc>Ttc | p.L174F |
PRAD | 6 | 162622178 | 162622178 | + | Silent | SNP | C | C | T | TCGA-EJ-7325-01B-11D-A32B-08 | TCGA-EJ-7325-10A-01D-A329-08 | g.chr6:162622178C>T | c.519G>A | c.(517-519)acG>acA | p.T173T |
PRAD | 6 | 162622263 | 162622263 | + | Missense_Mutation | SNP | C | C | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr6:162622263C>A | c.434G>T | c.(433-435)aGc>aTc | p.S145I |
PRAD | 6 | 162864373 | 162864373 | + | Missense_Mutation | SNP | C | C | T | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr6:162864373C>T | c.140G>A | c.(139-141)gGg>gAg | p.G47E |
READ | 6 | 161990401 | 161990401 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr6:161990401G>T | c.919C>A | c.(919-921)Ctg>Atg | p.L307M |
READ | 6 | 161990435 | 161990435 | + | Missense_Mutation | SNP | G | G | T | TCGA-F5-6571-01A-12D-1826-10 | TCGA-F5-6571-10A-01D-1826-10 | g.chr6:161990435G>T | c.885C>A | c.(883-885)aaC>aaA | p.N295K |
READ | 6 | 162475138 | 162475138 | + | Silent | SNP | G | G | A | TCGA-AG-3892-01A-01W-1073-09 | TCGA-AG-3892-10A-01W-1073-09 | g.chr6:162475138G>A | c.603C>T | c.(601-603)tgC>tgT | p.C201C |
READ | 6 | 162864376 | 162864376 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A00Y-01A-02W-A005-10 | TCGA-AG-A00Y-10A-01W-A005-10 | g.chr6:162864376G>T | c.137C>A | c.(136-138)gCa>gAa | p.A46E |
SARC | 6 | 162864388 | 162864388 | + | Missense_Mutation | SNP | C | C | T | TCGA-DX-A23Y-01A-11D-A27P-09 | TCGA-DX-A23Y-10A-01D-A27P-09 | g.chr6:162864388C>T | c.125G>A | c.(124-126)cGt>cAt | p.R42H |
SKCM | 6 | 161771200 | 161771200 | + | Silent | SNP | G | G | A | TCGA-D3-A51R-06A-11D-A25O-08 | TCGA-D3-A51R-10A-01D-A25O-08 | g.chr6:161771200G>A | c.1329C>T | c.(1327-1329)ctC>ctT | p.L443L |
SKCM | 6 | 161771215 | 161771215 | + | Silent | SNP | C | C | T | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr6:161771215C>T | c.1314G>A | c.(1312-1314)caG>caA | p.Q438Q |
SKCM | 6 | 161781175 | 161781175 | + | Silent | SNP | G | G | A | TCGA-D3-A3MV-06A-11D-A21A-08 | TCGA-D3-A3MV-10A-01D-A21A-08 | g.chr6:161781175G>A | c.1230C>T | c.(1228-1230)acC>acT | p.T410T |
SKCM | 6 | 161781186 | 161781186 | + | Missense_Mutation | SNP | A | A | G | TCGA-GF-A6C9-06A-11D-A30X-08 | TCGA-GF-A6C9-10A-01D-A30X-08 | g.chr6:161781186A>G | c.1219T>C | c.(1219-1221)Tcc>Ccc | p.S407P |
SKCM | 6 | 161807861 | 161807861 | + | Missense_Mutation | SNP | T | T | C | TCGA-EE-A29M-06A-11D-A196-08 | TCGA-EE-A29M-10A-01D-A198-08 | g.chr6:161807861T>C | c.1132A>G | c.(1132-1134)Agt>Ggt | p.S378G |
SKCM | 6 | 161807882 | 161807882 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MU-06A-21D-A196-08 | TCGA-EE-A2MU-10A-01D-A198-08 | g.chr6:161807882C>T | c.1111G>A | c.(1111-1113)Gcg>Acg | p.A371T |
SKCM | 6 | 161969941 | 161969941 | + | Missense_Mutation | SNP | G | G | A | TCGA-FR-A3YO-06A-11D-A23B-08 | TCGA-FR-A3YO-10A-01D-A23B-08 | g.chr6:161969941G>A | c.1028C>T | c.(1027-1029)cCg>cTg | p.P343L |
SKCM | 6 | 161969965 | 161969965 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2GR-06A-11D-A197-08 | TCGA-EE-A2GR-10A-01D-A199-08 | g.chr6:161969965G>A | c.1004C>T | c.(1003-1005)cCt>cTt | p.P335L |
SKCM | 6 | 161990439 | 161990439 | + | Missense_Mutation | SNP | G | G | A | TCGA-ER-A2NH-06A-11D-A196-08 | TCGA-ER-A2NH-10A-01D-A198-08 | g.chr6:161990439G>A | c.881C>T | c.(880-882)cCc>cTc | p.P294L |
SKCM | 6 | 162206911 | 162206911 | + | Missense_Mutation | SNP | G | G | A | TCGA-OD-A75X-06A-12D-A32N-08 | TCGA-OD-A75X-10A-01D-A32N-08 | g.chr6:162206911G>A | c.764C>T | c.(763-765)tCc>tTc | p.S255F |
SKCM | 6 | 162394441 | 162394441 | + | Silent | SNP | G | G | A | TCGA-FS-A1Z3-06A-11D-A197-08 | TCGA-FS-A1Z3-10A-01D-A199-08 | g.chr6:162394441G>A | c.627C>T | c.(625-627)ttC>ttT | p.F209F |
SKCM | 6 | 162622179 | 162622179 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3J5-06A-11D-A20D-08 | TCGA-EE-A3J5-10A-01D-A20D-08 | g.chr6:162622179G>A | c.518C>T | c.(517-519)aCg>aTg | p.T173M |
SKCM | 6 | 162622218 | 162622218 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29S-06A-11D-A197-08 | TCGA-EE-A29S-10A-01D-A199-08 | g.chr6:162622218C>T | c.479G>A | c.(478-480)gGa>gAa | p.G160E |
SKCM | 6 | 162622220 | 162622220 | + | Silent | SNP | C | C | T | TCGA-EE-A2MJ-06A-11D-A197-08 | TCGA-EE-A2MJ-10A-01D-A199-08 | g.chr6:162622220C>T | c.477G>A | c.(475-477)ccG>ccA | p.P159P |
SKCM | 6 | 162622263 | 162622263 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29E-06A-11D-A197-08 | TCGA-EE-A29E-10A-01D-A199-08 | g.chr6:162622263C>T | c.434G>A | c.(433-435)aGc>aAc | p.S145N |
SKCM | 6 | 162683579 | 162683579 | + | Silent | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr6:162683579G>A | c.390C>T | c.(388-390)gaC>gaT | p.D130D |
SKCM | 6 | 162683585 | 162683585 | + | Silent | SNP | C | C | T | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr6:162683585C>T | c.384G>A | c.(382-384)agG>agA | p.R128R |
SKCM | 6 | 162864378 | 162864378 | + | Silent | SNP | G | G | A | TCGA-D3-A51G-06A-11D-A25O-08 | TCGA-D3-A51G-10A-01D-A25O-08 | g.chr6:162864378G>A | c.135C>T | c.(133-135)ttC>ttT | p.F45F |
SKCM | 6 | 162864403 | 162864403 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MK-06A-11D-A196-08 | TCGA-EE-A2MK-10A-01D-A198-08 | g.chr6:162864403G>A | c.110C>T | c.(109-111)cCg>cTg | p.P37L |
SKCM | 6 | 162864441 | 162864441 | + | Silent | SNP | G | G | A | TCGA-GF-A6C9-06A-11D-A30X-08 | TCGA-GF-A6C9-10A-01D-A30X-08 | g.chr6:162864441G>A | c.72C>T | c.(70-72)ttC>ttT | p.F24F |