• TCGA
  • ICGC
  • CGAP
  • IntOGen
  • BioMuta

  
TCGA
ProjectGenome ChangecDNA ChangeCodon ChangeProtein ChangeChrStartEndStrandVariant ClassificationVariant TypeTumor Sample BarcodeMatched Norm Sample Barcode
BLCA8:74205835 C>Tc.13 G>Ac. (13-15)Gaa>Aaap.E5K87420583574205835+Splice_SiteSNPTCGA-DK-A1AC-01A-11D-A13W-08TCGA-DK-A1AC-10A-01D-A13W-08
BRCA8:74204933 G>Tc.114 C>Ac. (112-114)gc C>gcAp.A38A87420493374204933+SilentSNPTCGA-A8-A06Z-01A-11W-A019-09TCGA-A8-A06Z-10A-01W-A021-09
BRCA8:74205837 A>Cc.11 T>Gc. (10-12)gTa>gGap.V4G87420583774205837+Missense_MutationSNPTCGA-AN-A0FX-01A-11W-A050-09TCGA-AN-A0FX-10A-01W-A055-09
BRCA8:74204479 G>Ac.285 C>Tc. (283-285)at C>atTp.I95I87420447974204479+SilentSNPTCGA-B6-A0WZ-01A-11D-A10G-09TCGA-B6-A0WZ-10A-01D-A10G-09
CESC8:74203306 G>Ac.720 C>Tc. (718-720)at C>atTp.I240I87420330674203306+SilentSNPTCGA-EK-A2PM-01A-11D-A18J-09TCGA-EK-A2PM-10A-01D-A18J-09
COAD8:74204982 C>Tc.65 G>Ac. (64-66)cGa>cAap.R22Q87420498274204982+Missense_MutationSNPTCGA-AA-3811-01A-01W-0995-10TCGA-AA-3811-10A-01W-0995-10
COAD8:74204972 G>Ac.75 C>Tc. (73-75)tt C>ttTp.F25F87420497274204972+SilentSNPTCGA-AA-3984-01A-02W-0995-10TCGA-AA-3984-10A-01W-0999-10
COADREAD8:74204982 C>Tc.65 G>Ac. (64-66)cGa>cAap.R22Q87420498274204982+Missense_MutationSNPTCGA-AA-3811-01A-01W-0995-10TCGA-AA-3811-10A-01W-0995-10
COADREAD8:74204972 G>Ac.75 C>Tc. (73-75)tt C>ttTp.F25F87420497274204972+SilentSNPTCGA-AA-3984-01A-02W-0995-10TCGA-AA-3984-10A-01W-0999-10
DLBC8:74204061 G>Cc.375 C>Gc. (373-375)ct C>ctGp.L125L87420406174204061+SilentSNPTCGA-GS-A9TW-01A-11D-A382-10TCGA-GS-A9TW-10A-01D-A385-10
GBM8:74205020_74205022delCTTc.25_27delAAGc. (25-27)aagdelp.K9del87420502074205022+In_Frame_DelDELTCGA-06-0743-01A-01D-1492-08TCGA-06-0743-10A-01D-1492-08
GBMLGG8:74205020_74205022delCTTc.25_27delAAGc. (25-27)aagdelp.K9del87420502074205022+In_Frame_DelDELTCGA-06-0743-01A-01D-1492-08TCGA-06-0743-10A-01D-1492-08
KIPAN8:74204500 T>Ac.264 A>Tc. (262-264)aa A>aaTp.K88N87420450074204500+Missense_MutationSNPTCGA-BP-4782-01A-02D-1421-08TCGA-BP-4782-11A-01D-1421-08
KIRC8:74204500 T>Ac.264 A>Tc. (262-264)aa A>aaTp.K88N87420450074204500+Missense_MutationSNPTCGA-BP-4782-01A-02D-1421-08TCGA-BP-4782-11A-01D-1421-08
LUSC8:74203803 C>Gc.522 G>Cc. (520-522)tt G>ttCp.L174F87420380374203803+Missense_MutationSNPTCGA-22-5489-01A-01D-1632-08TCGA-22-5489-11A-01D-1632-08
PRAD8:74205006 A>Cc.41 T>Gc. (40-42)gTg>gGgp.V14G87420500674205006+Missense_MutationSNPTCGA-KK-A8IC-01A-11D-A364-08TCGA-KK-A8IC-11A-12D-A362-08
SARC8:74203808 C>Tc.517 G>Ac. (517-519)Gct>Actp.A173T87420380874203808+Missense_MutationSNPTCGA-IE-A4EJ-01A-11D-A24N-09TCGA-IE-A4EJ-10A-01D-A24N-09
SKCM8:74204012 A>Tc.424 T>Ac. (424-426)Tgg>Aggp.W142R87420401274204012+Missense_MutationSNPTCGA-EB-A4P0-01A-41D-A25O-08TCGA-EB-A4P0-10A-01D-A25O-08
SKCM8:74203428 G>Ac.598 C>Tc. (598-600)Cgc>Tgcp.R200C87420342874203428+Missense_MutationSNPTCGA-FS-A1YW-06A-11D-A197-08TCGA-FS-A1YW-10A-01D-A199-08
STAD8:74203895 A>Gc.430 T>Cc. (430-432)Tac>Cacp.Y144H87420389574203895+Splice_SiteSNPTCGA-BR-6452-01A-12D-1800-08TCGA-BR-6452-10A-01D-1800-08
STES8:74203895 A>Gc.430 T>Cc. (430-432)Tac>Cacp.Y144H87420389574203895+Splice_SiteSNPTCGA-BR-6452-01A-12D-1800-08TCGA-BR-6452-10A-01D-1800-08
UCEC8:74205017 C>Tc.30 G>Ac. (28-30)ga G>gaAp.E10E87420501774205017+SilentSNPTCGA-B5-A0JY-01A-11D-A10B-09TCGA-B5-A0JY-10A-01D-A10O-09
UCEC8:74204024 G>Ac.412 C>Tc. (412-414)Cca>Tcap.P138S87420402474204024+Missense_MutationSNPTCGA-D1-A103-01A-11D-A10M-09TCGA-D1-A103-10A-01D-A10M-09


ICGC
MutationProjectAA MutationCDS MutationChromosomeStartEndTypeConsequence
MU23109BLCA-CNI55I165 C>T87420447974204479Single base substitutionSynonymous_variant
MU23109BLCA-CNI95I285 C>T87420447974204479Single base substitutionSynonymous_variant
MU5076301BLCA-USE5K13 G>A87420583574205835Single base substitutionMissense_variant
MU1779834BRCA-EUR3Q8 G>A87420463674204636Single base substitutionMissense_variant
MU1779834BRCA-EUR43Q128 G>A87420463674204636Single base substitutionMissense_variant
MU23109BRCA-USI55I165 C>T87420447974204479Single base substitutionSynonymous_variant
MU23109BRCA-USI95I285 C>T87420447974204479Single base substitutionSynonymous_variant
MU42040BRCA-USV4G11 T>G87420583774205837Single base substitutionMissense_variant
MU12354BRCA-USA38A114 C>A87420493374204933Single base substitutionSynonymous_variant
MU29218745CESC-USI200I600 C>T87420330674203306Single base substitutionSynonymous_variant
MU29218745CESC-USI240I720 C>T87420330674203306Single base substitutionSynonymous_variant
MU103494COAD-USR117C349 C>T87420385674203856Single base substitutionMissense_variant
MU103494COAD-USR157C469 C>T87420385674203856Single base substitutionMissense_variant
MU158077COAD-USK40Q118 A>C87420492974204929Single base substitutionMissense_variant
MU48967798COCA-CNK125Q373 A>C87420383274203832Single base substitutionMissense_variant
MU48967798COCA-CNK165Q493 A>C87420383274203832Single base substitutionMissense_variant
MU595091GBM-USK987420502074205022Deletion of <=200bpInframe_deletion
MU624873KIRC-USK48N144 A>T87420450074204500Single base substitutionMissense_variant
MU624873KIRC-USK88N264 A>T87420450074204500Single base substitutionMissense_variant
MU595091LGG-USK987420502074205022Deletion of <=200bpInframe_deletion
MU1302941LUSC-USL134F402 G>C87420380374203803Single base substitutionMissense_variant
MU1302941LUSC-USL174F522 G>C87420380374203803Single base substitutionMissense_variant
MU595091ORCA-INK987420502074205022Deletion of <=200bpInframe_deletion
MU3880021OV-AUT130T390 A>G87420381574203815Single base substitutionSynonymous_variant
MU3880021OV-AUT170T510 A>G87420381574203815Single base substitutionSynonymous_variant
MU68242711PBCA-DEK29N87 G>T87420496074204960Single base substitutionMissense_variant
MU1779834READ-USR3Q8 G>A87420463674204636Single base substitutionMissense_variant
MU1779834READ-USR43Q128 G>A87420463674204636Single base substitutionMissense_variant
MU4438966SKCM-USR160C478 C>T87420342874203428Single base substitutionMissense_variant
MU4438966SKCM-USR200C598 C>T87420342874203428Single base substitutionMissense_variant
MU4407300SKCM-USW102R304 T>A87420401274204012Single base substitutionMissense_variant
MU4407300SKCM-USW142R424 T>A87420401274204012Single base substitutionMissense_variant
MU6381749STAD-USY104H310 T>C87420389574203895Single base substitutionMissense_variant
MU6381749STAD-USY144H430 T>C87420389574203895Single base substitutionMissense_variant
MU1986112UCEC-USP98S292 C>T87420402474204024Single base substitutionMissense_variant
MU1986112UCEC-USP138S412 C>T87420402474204024Single base substitutionMissense_variant
MU1849977UCEC-USE10E30 G>A87420501774205017Single base substitutionSynonymous_variant


CGAP
UniGeneCytobandOMIMSNP
Hs.4212578q21.11 6041662392023|CGAP|BC006095|C/T|coding|Pro138Ser|421|Candidate, 2392023|CGAP|BC008850|C/T|coding|Pro138Ser|458|Candidate, 2392023|CGAP|BC009599|C/T|coding|Pro138Ser|433|Candidate, 2392023|CGAP|BC071671|C/T|coding|Pro138Ser|414|Candidate, 2392023|CGAP|BC071894|C/T|coding|Pro138Ser|418|Candidate, 2392023|CGAP|BC071895|C/T|coding|Pro138Ser|416|Candidate, 2392023|CGAP|BC087837|C/T|coding|Pro138Ser|417|Candidate
Hs.5718418q21.11 6041662392023|CGAP|BC006095|C/T|coding|Pro138Ser|421|Candidate, 2392023|CGAP|BC008850|C/T|coding|Pro138Ser|458|Candidate, 2392023|CGAP|BC009599|C/T|coding|Pro138Ser|433|Candidate, 2392023|CGAP|BC071671|C/T|coding|Pro138Ser|414|Candidate, 2392023|CGAP|BC071894|C/T|coding|Pro138Ser|418|Candidate, 2392023|CGAP|BC071895|C/T|coding|Pro138Ser|416|Candidate, 2392023|CGAP|BC087837|C/T|coding|Pro138Ser|417|Candidate


IntOGen
CancerMutation AAcDNAChrPositionConsequence
BRCAp.V4Gc.11 T>G874205837Missense
BRCAp.A38Ac.114 C>A874204933Synonymous
BRCAp.I95Ic.285 C>T874204479Synonymous
CLLp.G183Cc.547 G>T874203479Missense
CMp.E2Kc.4 G>A874205844Missense
CMp.R200Cc.598 C>T874203428Missense
CMp.R200Cc.598 C>T874203428Missense
CMp.P210Pc.630 C>T874203396Synonymous
ESCAp.Y182_G183delins*c.546_547delinsAA874203479MultiAAMissense
GBMp.K9delKc.25_27delAAG874205020InFrameDeletion
LGGp.K9delKc.25_27delAAG874205020InFrameDeletion
LUADp.V4Lc.10 G>T874205838Missense
LUSCp.L174Fc.522 G>C874203803Missense
NBp.Y144Cc.431 A>G874203894Missense
RCCCp.K88Nc.264 A>T874204500Missense


BioMuta
PositionRefVarPosition (AA)Ref (AA)Var (AA)Cancer TypeFunctionReferences
40KQ118ACDOID:1521 / Cecum cancer [Cecca]Loss|Ubiquitylation-
88KN264ATDOID:263 / Kidney cancer [Kidca]Loss|Ubiquitylation-
22RQ65GADOID:219 / Colon cancer [Colca]--
27EK79GADOID:3571 / Liver cancer [Livca]- 23788652
43RQ128GADOID:1993 / Rectum cancer [Recca]--
157RC469CTDOID:1521 / Cecum cancer [Cecca]Loss|Binding Site-
138PS412CTDOID:363 / Uterine cancer [Uteca]Gain|Phosphorylation-
3GV8GTDOID:1324 / Lung cancer [Lunca]- 22980975
4VG11TGDOID:1612 / Breast cancer [BRCA]--
144YC431AGDOID:1192 / Peripheral nervous system neoplasm [PNSN]- 23334666
88KN264ATDOID:263 / Kidney cancer [Kidca]Loss|Ubiquitylation-
174LF522GCDOID:1324 / Lung cancer [Lunca]Gain|Phosphorylation-
4VL10GTDOID:1324 / Lung cancer [Lunca]--
4VG11TGDOID:1612 / Breast cancer [BRCA]--
200RC598CTDOID:4159 / Skin cancer [Skica]--
174LF522GCDOID:1324 / Lung cancer [Lunca]Gain|Phosphorylation-
157RC469CTDOID:219 / Colon cancer [Colca]Loss|Binding Site-
144YH430TCDOID:10534 / Stomach cancer [Stoca]--
142WR424TADOID:4159 / Skin cancer [Skica]--
88KN264ATDOID:263 / Kidney cancer [Kidca]Loss|Ubiquitylation-
43RQ128GADOID:1993 / Rectum cancer [Recca]--
40KQ118ACDOID:219 / Colon cancer [Colca]Loss|Ubiquitylation-
5EK13GADOID:11054 / Urinary bladder cancer [UBC]--
4VG11TGDOID:1612 / Breast cancer [BRCA]--
138PS412CTDOID:363 / Uterine cancer [Uteca]Gain|Phosphorylation-
174LF522GCDOID:1324 / Lung cancer [Lunca]Gain|Phosphorylation-
144YH430TCDOID:10534 / Stomach cancer [Stoca]--
142WR424TADOID:4159 / Skin cancer [Skica]--
106RSTOP316CTDOID:4159 / Skin cancer [Skica]--
200RC598CTDOID:4159 / Skin cancer [Skica]--
43RQ128GADOID:1993 / Rectum cancer [Recca]--
174LF522GCDOID:1324 / Lung cancer [Lunca]Gain|Phosphorylation-
88KN264ATDOID:263 / Kidney cancer [Kidca]Loss|Ubiquitylation-
40KQ118ACDOID:219 / Colon cancer [Colca]Loss|Ubiquitylation-
157RC469CTDOID:219 / Colon cancer [Colca]Loss|Binding Site-
4VG11TGDOID:1612 / Breast cancer [BRCA]--
5EK13GADOID:11054 / Urinary bladder cancer [UBC]--
5EK13GADOID:11054 / Urinary bladder cancer [UBC]--
183GC547GTDOID:2531 / Hematologic cancer [Hemca]- 23415222