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 | 1 | 15956926 | 15956926 | + | Missense_Mutation | SNP | A | A | G | TCGA-XF-A9SJ-01A-11D-A391-08 | TCGA-XF-A9SJ-10A-01D-A394-08 | g.chr1:15956926A>G | c.375A>G | c.(373-375)atA>atG | p.I125M |
BLCA | 1 | 15956939 | 15956939 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-DK-A1AC-01A-11D-A13W-08 | TCGA-DK-A1AC-10A-01D-A13W-08 | g.chr1:15956939C>T | c.388C>T | c.(388-390)Cag>Tag | p.Q130* |
BLCA | 1 | 15959933 | 15959933 | + | Splice_Site | SNP | G | G | C | TCGA-FD-A3SN-01A-12D-A22Z-08 | TCGA-FD-A3SN-10A-01D-A22Z-08 | g.chr1:15959933G>C | | c.e4-1 | |
BLCA | 1 | 15960017 | 15960017 | + | Missense_Mutation | SNP | C | C | G | TCGA-MV-A51V-01A-11D-A26M-08 | TCGA-MV-A51V-10A-01D-A26K-08 | g.chr1:15960017C>G | c.589C>G | c.(589-591)Ccc>Gcc | p.P197A |
BLCA | 1 | 15978264 | 15978264 | + | Missense_Mutation | SNP | C | C | G | TCGA-XF-A9SL-01A-11D-A391-08 | TCGA-XF-A9SL-10A-01D-A394-08 | g.chr1:15978264C>G | c.1057C>G | c.(1057-1059)Ctt>Gtt | p.L353V |
BLCA | 1 | 15978267 | 15978267 | + | Missense_Mutation | SNP | C | C | G | TCGA-DK-A3IL-01A-11D-A20D-08 | TCGA-DK-A3IL-10A-01D-A20D-08 | g.chr1:15978267C>G | c.1060C>G | c.(1060-1062)Cct>Gct | p.P354A |
BLCA | 1 | 15978369 | 15978369 | + | Missense_Mutation | SNP | C | C | G | TCGA-FD-A3SN-01A-12D-A22Z-08 | TCGA-FD-A3SN-10A-01D-A22Z-08 | g.chr1:15978369C>G | c.1162C>G | c.(1162-1164)Caa>Gaa | p.Q388E |
BRCA | 1 | 15956963 | 15956963 | + | Missense_Mutation | SNP | C | C | G | TCGA-C8-A3M8-01A-11D-A20S-09 | TCGA-C8-A3M8-10A-01D-A20S-09 | g.chr1:15956963C>G | c.412C>G | c.(412-414)Ctc>Gtc | p.L138V |
BRCA | 1 | 15978378 | 15978378 | + | Missense_Mutation | SNP | G | G | T | TCGA-AO-A0J3-01A-11W-A050-09 | TCGA-AO-A0J3-10A-01W-A055-09 | g.chr1:15978378G>T | c.1171G>T | c.(1171-1173)Gca>Tca | p.A391S |
CESC | 1 | 15959933 | 15959933 | + | Splice_Site | SNP | G | G | T | TCGA-DS-A5RQ-01A-11D-A28B-09 | TCGA-DS-A5RQ-10A-01D-A28E-09 | g.chr1:15959933G>T | | c.e4-1 | |
CESC | 1 | 15978270 | 15978270 | + | Missense_Mutation | SNP | G | G | A | TCGA-UC-A7PF-01A-11D-A351-09 | TCGA-UC-A7PF-11A-31D-A351-09 | g.chr1:15978270G>A | c.1063G>A | c.(1063-1065)Gag>Aag | p.E355K |
CESC | 1 | 15978347 | 15978347 | + | Silent | SNP | C | C | T | TCGA-DS-A1OA-01A-11D-A16Y-08 | TCGA-DS-A1OA-10A-01D-A16Y-08 | g.chr1:15978347C>T | c.1140C>T | c.(1138-1140)gaC>gaT | p.D380D |
COAD | 1 | 15956855 | 15956855 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A022-01A-21W-A096-10 | TCGA-AA-A022-11A-11W-A096-10 | g.chr1:15956855C>T | c.304C>T | c.(304-306)Cct>Tct | p.P102S |
COAD | 1 | 15964830 | 15964830 | + | Missense_Mutation | SNP | A | A | T | TCGA-AA-3833-01A-01W-0900-09 | TCGA-AA-3833-10A-01W-0900-09 | g.chr1:15964830A>T | c.661A>T | c.(661-663)Ata>Tta | p.I221L |
COADREAD | 1 | 15956855 | 15956855 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A022-01A-21W-A096-10 | TCGA-AA-A022-11A-11W-A096-10 | g.chr1:15956855C>T | c.304C>T | c.(304-306)Cct>Tct | p.P102S |
COADREAD | 1 | 15964830 | 15964830 | + | Missense_Mutation | SNP | A | A | T | TCGA-AA-3833-01A-01W-0900-09 | TCGA-AA-3833-10A-01W-0900-09 | g.chr1:15964830A>T | c.661A>T | c.(661-663)Ata>Tta | p.I221L |
GBM | 1 | 15978327 | 15978327 | + | Silent | SNP | C | C | A | TCGA-19-1790-01B-01D-1353-08 | TCGA-19-1790-10B-01D-1353-08 | g.chr1:15978327C>A | c.1120C>A | c.(1120-1122)Cgg>Agg | p.R374R |
GBMLGG | 1 | 15956989 | 15956989 | + | Silent | SNP | G | G | A | TCGA-E1-5322-01A-01D-1468-08 | TCGA-E1-5322-10A-01D-1468-08 | g.chr1:15956989G>A | c.438G>A | c.(436-438)ccG>ccA | p.P146P |
GBMLGG | 1 | 15964861 | 15964861 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr1:15964861G>T | c.692G>T | c.(691-693)gGc>gTc | p.G231V |
GBMLGG | 1 | 15978327 | 15978327 | + | Silent | SNP | C | C | A | TCGA-19-1790-01B-01D-1353-08 | TCGA-19-1790-10B-01D-1353-08 | g.chr1:15978327C>A | c.1120C>A | c.(1120-1122)Cgg>Agg | p.R374R |
HNSC | 1 | 15956839 | 15956839 | + | Silent | SNP | C | C | T | TCGA-CN-6998-01A-23D-2012-08 | TCGA-CN-6998-10A-01D-2013-08 | g.chr1:15956839C>T | c.288C>T | c.(286-288)ttC>ttT | p.F96F |
HNSC | 1 | 15956910 | 15956910 | + | Missense_Mutation | SNP | C | C | T | TCGA-CV-6935-01A-11D-1912-08 | TCGA-CV-6935-10A-01D-1912-08 | g.chr1:15956910C>T | c.359C>T | c.(358-360)tCa>tTa | p.S120L |
HNSC | 1 | 15959965 | 15959965 | + | Silent | SNP | G | G | A | TCGA-CV-6954-01A-11D-1912-08 | TCGA-CV-6954-10A-01D-1912-08 | g.chr1:15959965G>A | c.537G>A | c.(535-537)caG>caA | p.Q179Q |
HNSC | 1 | 15983119 | 15983119 | + | Silent | SNP | G | G | A | TCGA-CV-6961-01A-21D-1912-08 | TCGA-CV-6961-10A-01D-1912-08 | g.chr1:15983119G>A | c.1191G>A | c.(1189-1191)caG>caA | p.Q397Q |
KIPAN | 1 | 15956839 | 15956839 | + | Silent | SNP | C | C | T | TCGA-IZ-8196-01A-11D-2396-08 | TCGA-IZ-8196-10A-01D-2396-08 | g.chr1:15956839C>T | c.288C>T | c.(286-288)ttC>ttT | p.F96F |
KIPAN | 1 | 15956850 | 15956850 | + | Missense_Mutation | SNP | C | C | A | TCGA-HE-7128-01A-11D-1961-08 | TCGA-HE-7128-10A-01D-1962-08 | g.chr1:15956850C>A | c.299C>A | c.(298-300)gCt>gAt | p.A100D |
KIPAN | 1 | 15957021 | 15957021 | + | Missense_Mutation | SNP | C | C | T | TCGA-A4-7288-01A-11D-2136-08 | TCGA-A4-7288-11A-01D-2136-08 | g.chr1:15957021C>T | c.470C>T | c.(469-471)cCa>cTa | p.P157L |
KIRP | 1 | 15956839 | 15956839 | + | Silent | SNP | C | C | T | TCGA-IZ-8196-01A-11D-2396-08 | TCGA-IZ-8196-10A-01D-2396-08 | g.chr1:15956839C>T | c.288C>T | c.(286-288)ttC>ttT | p.F96F |
KIRP | 1 | 15956850 | 15956850 | + | Missense_Mutation | SNP | C | C | A | TCGA-HE-7128-01A-11D-1961-08 | TCGA-HE-7128-10A-01D-1962-08 | g.chr1:15956850C>A | c.299C>A | c.(298-300)gCt>gAt | p.A100D |
KIRP | 1 | 15957021 | 15957021 | + | Missense_Mutation | SNP | C | C | T | TCGA-A4-7288-01A-11D-2136-08 | TCGA-A4-7288-11A-01D-2136-08 | g.chr1:15957021C>T | c.470C>T | c.(469-471)cCa>cTa | p.P157L |
LGG | 1 | 15956989 | 15956989 | + | Silent | SNP | G | G | A | TCGA-E1-5322-01A-01D-1468-08 | TCGA-E1-5322-10A-01D-1468-08 | g.chr1:15956989G>A | c.438G>A | c.(436-438)ccG>ccA | p.P146P |
LGG | 1 | 15964861 | 15964861 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr1:15964861G>T | c.692G>T | c.(691-693)gGc>gTc | p.G231V |
LIHC | 1 | 15959967 | 15959967 | + | Missense_Mutation | SNP | A | A | G | TCGA-DD-A39Y-01A-11D-A20W-10 | TCGA-DD-A39Y-11A-11D-A20W-10 | g.chr1:15959967A>G | c.539A>G | c.(538-540)cAg>cGg | p.Q180R |
LUAD | 1 | 15953187 | 15953187 | + | Silent | SNP | C | C | T | TCGA-91-6831-01A-11D-1855-08 | TCGA-91-6831-11A-02D-1855-08 | g.chr1:15953187C>T | c.162C>T | c.(160-162)ctC>ctT | p.L54L |
LUAD | 1 | 15956966 | 15956966 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-50-5051-01A-21D-1855-08 | TCGA-50-5051-10A-01D-1855-08 | g.chr1:15956966C>T | c.415C>T | c.(415-417)Cga>Tga | p.R139* |
LUAD | 1 | 15959945 | 15959945 | + | Missense_Mutation | SNP | A | A | G | TCGA-05-4427-01A-21D-1855-08 | TCGA-05-4427-10A-01D-1855-08 | g.chr1:15959945A>G | c.517A>G | c.(517-519)Aga>Gga | p.R173G |
LUAD | 1 | 15970134 | 15970134 | + | Missense_Mutation | SNP | G | G | T | TCGA-17-Z031-01A-01W-0746-08 | TCGA-17-Z031-11A-01W-0746-08 | g.chr1:15970134G>T | c.878G>T | c.(877-879)aGg>aTg | p.R293M |
LUSC | 1 | 15956822 | 15956822 | + | Missense_Mutation | SNP | T | T | G | TCGA-22-5482-01A-01D-1632-08 | TCGA-22-5482-11A-01D-1632-08 | g.chr1:15956822T>G | c.271T>G | c.(271-273)Tta>Gta | p.L91V |
LUSC | 1 | 15956921 | 15956921 | + | Missense_Mutation | SNP | G | G | C | TCGA-56-5897-01A-11D-1632-08 | TCGA-56-5897-10A-01D-1632-08 | g.chr1:15956921G>C | c.370G>C | c.(370-372)Gaa>Caa | p.E124Q |
OV | 1 | 15953195 | 15953195 | + | Missense_Mutation | SNP | A | A | G | TCGA-30-1856-01A-01W-0639-09 | TCGA-30-1856-10A-01W-0639-09 | g.chr1:15953195A>G | c.170A>G | c.(169-171)aAc>aGc | p.N57S |
OV | 1 | 15957017 | 15957017 | + | Missense_Mutation | SNP | A | A | T | TCGA-29-2434-01A-01D-1526-09 | TCGA-29-2434-10A-01D-1526-09 | g.chr1:15957017A>T | c.466A>T | c.(466-468)Aat>Tat | p.N156Y |
OV | 1 | 15964846 | 15964846 | + | Missense_Mutation | SNP | C | C | G | TCGA-30-1718-01A-01W-0633-09 | TCGA-30-1718-10A-01W-0633-09 | g.chr1:15964846C>G | c.677C>G | c.(676-678)gCt>gGt | p.A226G |
PCPG | 1 | 15956918 | 15956918 | + | Missense_Mutation | SNP | G | G | A | TCGA-SR-A6MZ-01A-11D-A35I-08 | TCGA-SR-A6MZ-10A-01D-A35G-08 | g.chr1:15956918G>A | c.367G>A | c.(367-369)Gga>Aga | p.G123R |
SKCM | 1 | 15953255 | 15953255 | + | Missense_Mutation | SNP | A | A | T | TCGA-D3-A3ML-06A-11D-A21A-08 | TCGA-D3-A3ML-10A-01D-A21A-08 | g.chr1:15953255A>T | c.230A>T | c.(229-231)aAg>aTg | p.K77M |
SKCM | 1 | 15960018 | 15960018 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3J7-06A-11D-A20D-08 | TCGA-EE-A3J7-10A-01D-A20D-08 | g.chr1:15960018C>T | c.590C>T | c.(589-591)cCc>cTc | p.P197L |
SKCM | 1 | 15960047 | 15960047 | + | Missense_Mutation | SNP | G | G | A | TCGA-ER-A19P-06A-11D-A196-08 | TCGA-ER-A19P-10A-01D-A198-08 | g.chr1:15960047G>A | c.619G>A | c.(619-621)Gaa>Aaa | p.E207K |
SKCM | 1 | 15976263 | 15976263 | + | Missense_Mutation | SNP | T | T | G | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr1:15976263T>G | c.938T>G | c.(937-939)cTt>cGt | p.L313R |
SKCM | 1 | 15978205 | 15978205 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A5GO-06A-12D-A27K-08 | TCGA-D3-A5GO-10A-01D-A27N-08 | g.chr1:15978205C>T | c.998C>T | c.(997-999)tCc>tTc | p.S333F |
SKCM | 1 | 15978206 | 15978206 | + | Silent | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr1:15978206C>T | c.999C>T | c.(997-999)tcC>tcT | p.S333S |