Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CROCC

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000375541
Start 16953315:16953315(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs567924259
CDS Mutation c.3020G>A
AA Mutation p.Arg1007Gln(p.R1007Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000375541
Start 16958620:16958620(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374758748
CDS Mutation c.3902G>A
AA Mutation p.Arg1301Gln(p.R1301Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000375541
Start 16948422:16948422(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758565180
CDS Mutation c.2606G>A
AA Mutation p.Arg869His(p.R869H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000375541
Start 16930584:16930584(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745994746
CDS Mutation c.839G>A
AA Mutation p.Arg280His(p.R280H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000375541
Start 16940033:16940033(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1748C>T
AA Mutation p.Ala583Val(p.A583V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000375541
Start 16931315:16931315(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768236725
CDS Mutation c.874G>A
AA Mutation p.Glu292Lys(p.E292K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000375541
Start 16966428:16966428(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4717C>T
AA Mutation p.Arg1573Trp(p.R1573W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000375541
Start 16954280:16954280(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201086543
CDS Mutation c.3244C>T
AA Mutation p.Arg1082Trp(p.R1082W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000375541
Start 16936825:16936825(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs561750754
CDS Mutation c.1145C>T
AA Mutation p.Ala382Val(p.A382V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000375541
Start 16922798:16922798(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.196G>T
AA Mutation p.Val66Phe(p.V66F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000375541
Start 16924432:16924432(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761796681
CDS Mutation c.304G>A
AA Mutation p.Ala102Thr(p.A102T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000375541
Start 16930572:16930572(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755908527
CDS Mutation c.827C>T
AA Mutation p.Ala276Val(p.A276V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000375541
Start 16954329:16954329(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3293A>G
AA Mutation p.Asp1098Gly(p.D1098G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000375541
Start 16938987:16938987(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1453C>T
AA Mutation p.Arg485Trp(p.R485W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000375541
Start 16955454:16955454(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779341603
CDS Mutation c.3608G>A
AA Mutation p.Arg1203His(p.R1203H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000375541
Start 16954238:16954238(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3202G>A
AA Mutation p.Glu1068Lys(p.E1068K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000375541
Start 16954857:16954857(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374075325
CDS Mutation c.3445C>T
AA Mutation p.Arg1149Trp(p.R1149W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000375541
Start 16968342:16968342(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5000G>A
AA Mutation p.Arg1667His(p.R1667H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000375541
Start 16966068:16966068(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs146661921
CDS Mutation c.4645G>A
AA Mutation p.Ala1549Thr(p.A1549T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000375541
Start 16970424:16970424(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs182106939
CDS Mutation c.5623C>T
AA Mutation p.Arg1875Cys(p.R1875C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000375541
Start 16939906:16939906(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1621C>T
AA Mutation p.Arg541Cys(p.R541C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000375541
Start 16946878:16946878(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781364301
CDS Mutation c.2401C>T
AA Mutation p.Arg801Trp(p.R801W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000375541
Start 16930481:16930481(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.736G>T
AA Mutation p.Ala246Ser(p.A246S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000375541
Start 16931319:16931319(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776274168
CDS Mutation c.878A>G
AA Mutation p.His293Arg(p.H293R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000375541
Start 16944204:16944204(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776872732
CDS Mutation c.1913G>A
AA Mutation p.Arg638His(p.R638H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000375541
Start 16930547:16930547(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144174614
CDS Mutation c.802C>T
AA Mutation p.Arg268Cys(p.R268C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000375541
Start 16955355:16955355(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762876230
CDS Mutation c.3509G>A
AA Mutation p.Arg1170His(p.R1170H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000375541
Start 16965883:16965883(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4566G>T
AA Mutation p.Gln1522His(p.Q1522H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000375541
Start 16945467:16945467(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777660553
CDS Mutation c.1997G>T
AA Mutation p.Arg666Ile(p.R666I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000375541
Start 16958669:16958669(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3951G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000375541
Start 16969199:16969199(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143447514
CDS Mutation c.5160C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000375541
Start 16930435:16930435(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.690C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000375541
Start 16945543:16945543(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757341913
CDS Mutation c.2073C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000375541
Start 16924440:16924440(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774563422
CDS Mutation c.312C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000375541
Start 16931362:16931362(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.921G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000375541
Start 16924449:16924449(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148572053
CDS Mutation c.321C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000375541
Start 16937671:16937671(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1224T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000375541
Start 16936814:16936814(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1134G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000375541
Start 16929998:16929998(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.504G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000375541
Start 16958744:16958744(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4026G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence stop_gained
Transcription ID ENST00000375541
Start 16930463:16930463(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779871764
CDS Mutation c.718C>T
AA Mutation p.Arg240Ter(p.R240*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 42
Mutation Consequence stop_gained
Transcription ID ENST00000375541
Start 16930517:16930517(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs150645566
CDS Mutation c.772C>T
AA Mutation p.Arg258Ter(p.R258*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 43
Mutation Consequence stop_gained
Transcription ID ENST00000375541
Start 16966092:16966092(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4669C>T
AA Mutation p.Gln1557Ter(p.Q1557*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 44
Mutation Consequence frameshift_variant
Transcription ID ENST00000375541
Start 16940044:16940045(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.1761_1762dupCC
AA Mutation p.Gln588ProfsTer15(p.Q588Pfs*15)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> CROCC

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000375541
Start 16950971:16950971(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768170307
CDS Mutation c.2855G>A
AA Mutation p.Arg952Gln(p.R952Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000375541
Start 16951078:16951078(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs3969856
CDS Mutation c.2962C>T
AA Mutation p.Arg988Trp(p.R988W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000375541
Start 16936657:16936657(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.977G>T
AA Mutation p.Gly326Val(p.G326V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000375541
Start 16955359:16955359(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs150383004
CDS Mutation c.3513C>T
Mutation Classification Silent
Feature Type Transcript