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 |
ACC | 11 | 5701024 | 5701024 | + | Silent | SNP | C | C | T | TCGA-OR-A5K4-01A-11D-A29I-10 | TCGA-OR-A5K4-10A-01D-A29L-10 | g.chr11:5701024C>T | c.384G>A | c.(382-384)acG>acA | p.T128T |
BLCA | 11 | 5686256 | 5686256 | + | Missense_Mutation | SNP | G | G | A | TCGA-G2-A3IE-01A-11D-A20D-08 | TCGA-G2-A3IE-10A-01D-A20D-08 | g.chr11:5686256G>A | c.1265C>T | c.(1264-1266)tCt>tTt | p.S422F |
BLCA | 11 | 5686559 | 5686559 | + | Missense_Mutation | SNP | C | C | T | TCGA-GC-A3WC-01A-31D-A22Z-08 | TCGA-GC-A3WC-10A-01D-A22Z-08 | g.chr11:5686559C>T | c.962G>A | c.(961-963)aGc>aAc | p.S321N |
BLCA | 11 | 5687293 | 5687293 | + | Missense_Mutation | SNP | C | C | G | TCGA-GD-A2C5-01A-12D-A17V-08 | TCGA-GD-A2C5-10A-01D-A17V-08 | g.chr11:5687293C>G | c.786G>C | c.(784-786)ttG>ttC | p.L262F |
BRCA | 11 | 5686165 | 5686165 | + | Silent | SNP | G | G | A | TCGA-AO-A0JE-01A-11W-A071-09 | TCGA-AO-A0JE-10A-01W-A071-09 | g.chr11:5686165G>A | c.1356C>T | c.(1354-1356)ttC>ttT | p.F452F |
BRCA | 11 | 5686469 | 5686469 | + | Missense_Mutation | SNP | G | G | C | TCGA-BH-A0B5-01A-11D-A12Q-09 | TCGA-BH-A0B5-11A-23W-A14O-09 | g.chr11:5686469G>C | c.1052C>G | c.(1051-1053)tCt>tGt | p.S351C |
CESC | 11 | 5686913 | 5686913 | + | Splice_Site | SNP | C | C | G | TCGA-RA-A741-01A-11D-A33O-09 | TCGA-RA-A741-10B-01D-A33O-09 | g.chr11:5686913C>G | | c.e7-1 | |
CESC | 11 | 5701146 | 5701146 | + | Missense_Mutation | SNP | C | C | G | TCGA-Q1-A73O-01A-11D-A32I-09 | TCGA-Q1-A73O-10B-01D-A32I-09 | g.chr11:5701146C>G | c.262G>C | c.(262-264)Gag>Cag | p.E88Q |
CHOL | 11 | 5686556 | 5686556 | + | Missense_Mutation | SNP | G | G | T | TCGA-ZH-A8Y8-01A-51D-A417-09 | TCGA-ZH-A8Y8-10A-01D-A41A-09 | g.chr11:5686556G>T | c.965C>A | c.(964-966)tCt>tAt | p.S322Y |
COAD | 11 | 5686181 | 5686181 | + | Missense_Mutation | SNP | C | C | T | TCGA-CM-5861-01A-01D-1650-10 | TCGA-CM-5861-10A-01D-1650-10 | g.chr11:5686181C>T | c.1340G>A | c.(1339-1341)tGc>tAc | p.C447Y |
COAD | 11 | 5686249 | 5686249 | + | Silent | SNP | A | A | C | TCGA-CM-6171-01A-11D-1650-10 | TCGA-CM-6171-10A-01D-1650-10 | g.chr11:5686249A>C | c.1272T>G | c.(1270-1272)ccT>ccG | p.P424P |
COAD | 11 | 5686351 | 5686352 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr11:5686351_5686352insT | c.1169_1170insA | c.(1168-1170)aatfs | p.N390fs |
COAD | 11 | 5686497 | 5686497 | + | Missense_Mutation | SNP | A | A | C | TCGA-A6-6141-01A-11D-1771-10 | TCGA-A6-6141-10A-01D-1771-10 | g.chr11:5686497A>C | c.1024T>G | c.(1024-1026)Ttc>Gtc | p.F342V |
COAD | 11 | 5686820 | 5686821 | + | Intron | INS | - | - | A | TCGA-AA-3492-01A-01D-1408-10 | TCGA-AA-3492-11A-01D-1408-10 | g.chr11:5686820_5686821insA | | | |
COAD | 11 | 5699635 | 5699635 | + | Silent | SNP | G | G | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr11:5699635G>T | c.543C>A | c.(541-543)gtC>gtA | p.V181V |
COAD | 11 | 5701287 | 5701287 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-6599-01A-11D-1771-10 | TCGA-AZ-6599-11A-01D-1771-10 | g.chr11:5701287C>T | c.121G>A | c.(121-123)Gca>Aca | p.A41T |
COAD | 11 | 5701287 | 5701287 | + | Missense_Mutation | SNP | C | C | T | TCGA-CM-4743-01A-01D-1719-10 | TCGA-CM-4743-10A-01D-1719-10 | g.chr11:5701287C>T | c.121G>A | c.(121-123)Gca>Aca | p.A41T |
COADREAD | 11 | 5686181 | 5686181 | + | Missense_Mutation | SNP | C | C | T | TCGA-CM-5861-01A-01D-1650-10 | TCGA-CM-5861-10A-01D-1650-10 | g.chr11:5686181C>T | c.1340G>A | c.(1339-1341)tGc>tAc | p.C447Y |
COADREAD | 11 | 5686249 | 5686249 | + | Silent | SNP | A | A | C | TCGA-CM-6171-01A-11D-1650-10 | TCGA-CM-6171-10A-01D-1650-10 | g.chr11:5686249A>C | c.1272T>G | c.(1270-1272)ccT>ccG | p.P424P |
COADREAD | 11 | 5686351 | 5686352 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr11:5686351_5686352insT | c.1169_1170insA | c.(1168-1170)aatfs | p.N390fs |
COADREAD | 11 | 5686497 | 5686497 | + | Missense_Mutation | SNP | A | A | C | TCGA-A6-6141-01A-11D-1771-10 | TCGA-A6-6141-10A-01D-1771-10 | g.chr11:5686497A>C | c.1024T>G | c.(1024-1026)Ttc>Gtc | p.F342V |
COADREAD | 11 | 5686820 | 5686821 | + | Intron | INS | - | - | A | TCGA-AA-3492-01A-01D-1408-10 | TCGA-AA-3492-11A-01D-1408-10 | g.chr11:5686820_5686821insA | | | |
COADREAD | 11 | 5699635 | 5699635 | + | Silent | SNP | G | G | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr11:5699635G>T | c.543C>A | c.(541-543)gtC>gtA | p.V181V |
COADREAD | 11 | 5701072 | 5701072 | + | Silent | SNP | G | G | T | TCGA-AG-3881-01A-01W-0899-10 | TCGA-AG-3881-10A-01W-0901-10 | g.chr11:5701072G>T | c.336C>A | c.(334-336)gtC>gtA | p.V112V |
COADREAD | 11 | 5701287 | 5701287 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-6599-01A-11D-1771-10 | TCGA-AZ-6599-11A-01D-1771-10 | g.chr11:5701287C>T | c.121G>A | c.(121-123)Gca>Aca | p.A41T |
COADREAD | 11 | 5701287 | 5701287 | + | Missense_Mutation | SNP | C | C | T | TCGA-CM-4743-01A-01D-1719-10 | TCGA-CM-4743-10A-01D-1719-10 | g.chr11:5701287C>T | c.121G>A | c.(121-123)Gca>Aca | p.A41T |
ESCA | 11 | 5686747 | 5686747 | + | Intron | SNP | G | G | T | TCGA-S8-A6BV-01A-21D-A31U-09 | TCGA-S8-A6BV-10A-01D-A31U-09 | g.chr11:5686747G>T | | | |
ESCA | 11 | 5701291 | 5701291 | + | Silent | SNP | G | G | T | TCGA-R6-A6XG-01B-11D-A33E-09 | TCGA-R6-A6XG-10A-01D-A33H-09 | g.chr11:5701291G>T | c.117C>A | c.(115-117)ctC>ctA | p.L39L |
GBM | 11 | 5699638 | 5699638 | + | Silent | SNP | G | G | A | TCGA-16-1045-01B-01W-0611-08 | TCGA-16-1045-10B-01W-0611-08 | g.chr11:5699638G>A | c.540C>T | c.(538-540)aaC>aaT | p.N180N |
GBMLGG | 11 | 5686810 | 5686810 | + | Intron | SNP | C | C | A | TCGA-VW-A8FI-01A-11D-A36O-08 | TCGA-VW-A8FI-10A-01D-A367-08 | g.chr11:5686810C>A | | | |
GBMLGG | 11 | 5688922 | 5688922 | + | Missense_Mutation | SNP | T | T | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr11:5688922T>G | c.764A>C | c.(763-765)aAa>aCa | p.K255T |
GBMLGG | 11 | 5699638 | 5699638 | + | Silent | SNP | G | G | A | TCGA-16-1045-01B-01W-0611-08 | TCGA-16-1045-10B-01W-0611-08 | g.chr11:5699638G>A | c.540C>T | c.(538-540)aaC>aaT | p.N180N |
GBMLGG | 11 | 5701232 | 5701232 | + | Missense_Mutation | SNP | C | C | T | TCGA-TQ-A7RR-01A-21D-A34A-08 | TCGA-TQ-A7RR-10A-01D-A34A-08 | g.chr11:5701232C>T | c.176G>A | c.(175-177)cGg>cAg | p.R59Q |
HNSC | 11 | 5686482 | 5686482 | + | Missense_Mutation | SNP | C | C | A | TCGA-CQ-5334-01A-01D-1683-08 | TCGA-CQ-5334-10A-01D-1683-08 | g.chr11:5686482C>A | c.1039G>T | c.(1039-1041)Ggc>Tgc | p.G347C |
HNSC | 11 | 5688930 | 5688930 | + | Silent | SNP | G | G | A | TCGA-CV-A6K1-01A-11D-A31L-08 | TCGA-CV-A6K1-10A-01D-A31J-08 | g.chr11:5688930G>A | c.756C>T | c.(754-756)ggC>ggT | p.G252G |
HNSC | 11 | 5699528 | 5699528 | + | Missense_Mutation | SNP | G | G | C | TCGA-DQ-5631-01A-01D-1870-08 | TCGA-DQ-5631-10A-01D-1870-08 | g.chr11:5699528G>C | c.650C>G | c.(649-651)tCt>tGt | p.S217C |
HNSC | 11 | 5699621 | 5699621 | + | Missense_Mutation | SNP | T | T | C | TCGA-CV-7255-01A-11D-2012-08 | TCGA-CV-7255-10A-01D-2013-08 | g.chr11:5699621T>C | c.557A>G | c.(556-558)gAg>gGg | p.E186G |
HNSC | 11 | 5699628 | 5699628 | + | Missense_Mutation | SNP | C | C | G | TCGA-BA-A6DJ-01A-11D-A30E-08 | TCGA-BA-A6DJ-10A-01D-A30H-08 | g.chr11:5699628C>G | c.550G>C | c.(550-552)Gat>Cat | p.D184H |
HNSC | 11 | 5701005 | 5701005 | + | Missense_Mutation | SNP | C | C | A | TCGA-CR-7399-01A-11D-2012-08 | TCGA-CR-7399-10A-01D-2013-08 | g.chr11:5701005C>A | c.403G>T | c.(403-405)Gcc>Tcc | p.A135S |
HNSC | 11 | 5701153 | 5701153 | + | Missense_Mutation | SNP | C | C | G | TCGA-CV-A6K2-01A-11D-A31L-08 | TCGA-CV-A6K2-10A-01D-A31J-08 | g.chr11:5701153C>G | c.255G>C | c.(253-255)ttG>ttC | p.L85F |
HNSC | 11 | 5701231 | 5701231 | + | Silent | SNP | C | C | G | TCGA-CN-4723-01A-01D-1434-08 | TCGA-CN-4723-10A-01D-1434-08 | g.chr11:5701231C>G | c.177G>C | c.(175-177)cgG>cgC | p.R59R |
HNSC | 11 | 5701271 | 5701271 | + | Missense_Mutation | SNP | G | G | C | TCGA-MT-A67F-01A-11D-A30E-08 | TCGA-MT-A67F-10A-01D-A30H-08 | g.chr11:5701271G>C | c.137C>G | c.(136-138)tCc>tGc | p.S46C |
KIPAN | 11 | 5687233 | 5687233 | + | Silent | SNP | T | T | C | TCGA-BP-4970-01A-01D-1462-08 | TCGA-BP-4970-11A-01D-1462-08 | g.chr11:5687233T>C | c.846A>G | c.(844-846)aaA>aaG | p.K282K |
KIPAN | 11 | 5699642 | 5699642 | + | Missense_Mutation | SNP | G | G | C | TCGA-B0-5695-01A-11D-1534-10 | TCGA-B0-5695-11A-01D-1534-10 | g.chr11:5699642G>C | c.536C>G | c.(535-537)aCc>aGc | p.T179S |
KIRC | 11 | 5687233 | 5687233 | + | Silent | SNP | T | T | C | TCGA-BP-4970-01A-01D-1462-08 | TCGA-BP-4970-11A-01D-1462-08 | g.chr11:5687233T>C | c.846A>G | c.(844-846)aaA>aaG | p.K282K |
KIRC | 11 | 5699642 | 5699642 | + | Missense_Mutation | SNP | G | G | C | TCGA-B0-5695-01A-11D-1534-10 | TCGA-B0-5695-11A-01D-1534-10 | g.chr11:5699642G>C | c.536C>G | c.(535-537)aCc>aGc | p.T179S |
LGG | 11 | 5686810 | 5686810 | + | Intron | SNP | C | C | A | TCGA-VW-A8FI-01A-11D-A36O-08 | TCGA-VW-A8FI-10A-01D-A367-08 | g.chr11:5686810C>A | | | |
LGG | 11 | 5688922 | 5688922 | + | Missense_Mutation | SNP | T | T | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr11:5688922T>G | c.764A>C | c.(763-765)aAa>aCa | p.K255T |
LGG | 11 | 5701232 | 5701232 | + | Missense_Mutation | SNP | C | C | T | TCGA-TQ-A7RR-01A-21D-A34A-08 | TCGA-TQ-A7RR-10A-01D-A34A-08 | g.chr11:5701232C>T | c.176G>A | c.(175-177)cGg>cAg | p.R59Q |
LIHC | 11 | 5686301 | 5686301 | + | Missense_Mutation | SNP | C | C | A | TCGA-ZS-A9CD-01A-11D-A36X-10 | TCGA-ZS-A9CD-10A-01D-A370-10 | g.chr11:5686301C>A | c.1220G>T | c.(1219-1221)gGa>gTa | p.G407V |
LUAD | 11 | 5686301 | 5686301 | + | Missense_Mutation | SNP | C | C | A | TCGA-71-8520-01A-11D-2393-08 | TCGA-71-8520-10A-01D-2393-08 | g.chr11:5686301C>A | c.1220G>T | c.(1219-1221)gGa>gTa | p.G407V |
LUAD | 11 | 5687286 | 5687286 | + | Missense_Mutation | SNP | G | G | T | TCGA-55-8616-01A-11D-2393-08 | TCGA-55-8616-10A-01D-2393-08 | g.chr11:5687286G>T | c.793C>A | c.(793-795)Cca>Aca | p.P265T |
LUAD | 11 | 5699520 | 5699520 | + | Missense_Mutation | SNP | C | C | G | TCGA-17-Z056-01A-01W-0747-08 | TCGA-17-Z056-11A-01W-0747-08 | g.chr11:5699520C>G | c.658G>C | c.(658-660)Gag>Cag | p.E220Q |
LUSC | 11 | 5686040 | 5686040 | + | Nonstop_Mutation | SNP | C | C | G | TCGA-66-2758-01A-02D-1522-08 | TCGA-66-2758-11A-01D-1522-08 | g.chr11:5686040C>G | c.1481G>C | c.(1480-1482)tGa>tCa | p.*494S |
LUSC | 11 | 5686453 | 5686453 | + | Silent | SNP | T | T | C | TCGA-60-2698-01A-01D-1522-08 | TCGA-60-2698-11A-01D-1522-08 | g.chr11:5686453T>C | c.1068A>G | c.(1066-1068)tcA>tcG | p.S356S |
LUSC | 11 | 5701330 | 5701330 | + | Silent | SNP | C | C | T | TCGA-46-6026-01A-11D-1817-08 | TCGA-46-6026-10A-01D-1817-08 | g.chr11:5701330C>T | c.78G>A | c.(76-78)ctG>ctA | p.L26L |
OV | 11 | 5699665 | 5699665 | + | Splice_Site | SNP | C | C | T | TCGA-20-1686-01A-01W-0633-09 | TCGA-20-1686-10A-01W-0633-09 | g.chr11:5699665C>T | | c.e4-1 | |
OV | 11 | 5701015 | 5701015 | + | Silent | SNP | T | T | C | TCGA-36-2552-01A-01D-1526-09 | TCGA-36-2552-10A-01D-1526-09 | g.chr11:5701015T>C | c.393A>G | c.(391-393)acA>acG | p.T131T |
OV | 11 | 5701286 | 5701286 | + | Missense_Mutation | SNP | G | G | A | TCGA-59-2348-01A-01W-0799-08 | TCGA-59-2348-11A-01W-0800-08 | g.chr11:5701286G>A | c.122C>T | c.(121-123)gCa>gTa | p.A41V |
PAAD | 11 | 5687305 | 5687305 | + | Missense_Mutation | SNP | C | C | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr11:5687305C>A | c.774G>T | c.(772-774)gaG>gaT | p.E258D |
PAAD | 11 | 5699533 | 5699533 | + | Silent | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr11:5699533C>T | c.645G>A | c.(643-645)acG>acA | p.T215T |
PRAD | 11 | 5686330 | 5686330 | + | Silent | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr11:5686330G>A | c.1191C>T | c.(1189-1191)taC>taT | p.Y397Y |
PRAD | 11 | 5686351 | 5686352 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-CH-5769-01A-11D-1576-08 | TCGA-CH-5769-11A-01D-1576-08 | g.chr11:5686351_5686352insT | c.1169_1170insA | c.(1168-1170)aatfs | p.N390fs |
PRAD | 11 | 5686409 | 5686409 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-EJ-8474-01A-11D-2395-08 | TCGA-EJ-8474-10A-01D-2395-08 | g.chr11:5686409C>T | c.1112G>A | c.(1111-1113)tGg>tAg | p.W371* |
PRAD | 11 | 5686494 | 5686494 | + | Missense_Mutation | SNP | T | T | A | TCGA-V1-A9OX-01A-11D-A41K-08 | TCGA-V1-A9OX-10A-01D-A41N-08 | g.chr11:5686494T>A | c.1027A>T | c.(1027-1029)Aat>Tat | p.N343Y |
PRAD | 11 | 5701211 | 5701211 | + | Missense_Mutation | SNP | T | T | G | TCGA-HC-8256-01A-11D-2260-08 | TCGA-HC-8256-10A-01D-2260-08 | g.chr11:5701211T>G | c.197A>C | c.(196-198)aAc>aCc | p.N66T |
PRAD | 11 | 5701287 | 5701287 | + | Missense_Mutation | SNP | C | C | T | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr11:5701287C>T | c.121G>A | c.(121-123)Gca>Aca | p.A41T |
READ | 11 | 5701072 | 5701072 | + | Silent | SNP | G | G | T | TCGA-AG-3881-01A-01W-0899-10 | TCGA-AG-3881-10A-01W-0901-10 | g.chr11:5701072G>T | c.336C>A | c.(334-336)gtC>gtA | p.V112V |
SKCM | 11 | 5686212 | 5686212 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A51T-06A-11D-A25O-08 | TCGA-D3-A51T-10A-01D-A25O-08 | g.chr11:5686212G>A | c.1309C>T | c.(1309-1311)Cgt>Tgt | p.R437C |
SKCM | 11 | 5686228 | 5686228 | + | Silent | SNP | C | C | T | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr11:5686228C>T | c.1293G>A | c.(1291-1293)gtG>gtA | p.V431V |
SKCM | 11 | 5686459 | 5686459 | + | Silent | SNP | G | G | A | TCGA-EE-A180-06A-11D-A21A-08 | TCGA-EE-A180-10B-01D-A21A-08 | g.chr11:5686459G>A | c.1062C>T | c.(1060-1062)atC>atT | p.I354I |
SKCM | 11 | 5686856 | 5686856 | + | Intron | SNP | G | G | A | TCGA-DA-A1I7-06A-22D-A197-08 | TCGA-DA-A1I7-10A-01D-A199-08 | g.chr11:5686856G>A | | | |
SKCM | 11 | 5687273 | 5687273 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr11:5687273G>A | c.806C>T | c.(805-807)cCa>cTa | p.P269L |