Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> GNAS

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000371085
Start 58909366:58909366(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs121913495
CDS Mutation c.602G>A
AA Mutation p.Arg201His(p.R201H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000371085
Start 58903684:58903684(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.325G>A
AA Mutation p.Ala109Thr(p.A109T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000371100
Start 58854368:58854368(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1103C>T
AA Mutation p.Ala368Val(p.A368V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000371085
Start 58910710:58910710(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1066C>T
AA Mutation p.Arg356Cys(p.R356C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000371100
Start 58854232:58854232(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773471190
CDS Mutation c.967G>A
AA Mutation p.Val323Ile(p.V323I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000371100
Start 58853311:58853311(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757200947
CDS Mutation c.46C>T
AA Mutation p.Arg16Cys(p.R16C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000371100
Start 58855243:58855243(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751987537
CDS Mutation c.1978C>T
AA Mutation p.Arg660Cys(p.R660C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000371085
Start 58909365:58909365(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs11554273
CDS Mutation c.601C>T
AA Mutation p.Arg201Cys(p.R201C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000371100
Start 58853369:58853369(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.104G>A
AA Mutation p.Gly35Glu(p.G35E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000371100
Start 58853272:58853272(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781303953
CDS Mutation c.7G>A
AA Mutation p.Val3Met(p.V3M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000371100
Start 58854152:58854152(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.887C>T
AA Mutation p.Thr296Met(p.T296M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000371100
Start 58855216:58855216(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1951G>A
AA Mutation p.Glu651Lys(p.E651K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000371100
Start 58855319:58855319(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2054G>A
AA Mutation p.Arg685His(p.R685H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000371100
Start 58854266:58854266(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs535138966
CDS Mutation c.1001G>A
AA Mutation p.Gly334Asp(p.G334D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000371100
Start 58854219:58854219(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.954C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 16
Mutation Consequence synonymous_variant
Transcription ID ENST00000371100
Start 58853313:58853313(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.48C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 17
Mutation Consequence synonymous_variant
Transcription ID ENST00000371100
Start 58854981:58854981(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1716C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 18
Mutation Consequence synonymous_variant
Transcription ID ENST00000371100
Start 58854234:58854234(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.969C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 19
Mutation Consequence stop_gained
Transcription ID ENST00000371100
Start 58855216:58855216(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1951G>T
AA Mutation p.Glu651Ter(p.E651*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> GNAS

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000371085
Start 58909366:58909366(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.602G>T
AA Mutation p.Arg201Leu(p.R201L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000371100
Start 58854286:58854286(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777234998
CDS Mutation c.1021G>A
AA Mutation p.Gly341Arg(p.G341R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000371100
Start 58855313:58855313(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374419453
CDS Mutation c.2048C>T
AA Mutation p.Thr683Met(p.T683M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000371100
Start 58855160:58855160(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1895G>A
AA Mutation p.Arg632His(p.R632H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000371100
Start 58853762:58853762(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.497T>G
AA Mutation p.Phe166Cys(p.F166C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000371100
Start 58854984:58854984(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753322339
CDS Mutation c.1719C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000371100
Start 58853313:58853313(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.48C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000371100
Start 58853916:58853916(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.651C>T
Mutation Classification Silent
Feature Type Transcript