Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> GAS2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000278187
Start 22755938:22755938(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.708G>T
AA Mutation p.Lys236Asn(p.K236N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000278187
Start 22726338:22726338(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.314G>A
AA Mutation p.Gly105Asp(p.G105D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000278187
Start 22674981:22674981(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.112G>A
AA Mutation p.Glu38Lys(p.E38K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000278187
Start 22755946:22755946(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.716T>G
AA Mutation p.Phe239Cys(p.F239C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000278187
Start 22726429:22726429(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.405T>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000278187
Start 22737724:22737724(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.429A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000278187
Start 22674992:22674992(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.123C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000278187
Start 22674962:22674962(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.93T>G
Mutation Classification Silent
Feature Type Transcript

Rectum Cancer: Gene >> GAS2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000278187
Start 22685707:22685707(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.185A>G
AA Mutation p.Asp62Gly(p.D62G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence stop_gained
Transcription ID ENST00000278187
Start 22755924:22755924(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767538779
CDS Mutation c.694C>T
AA Mutation p.Arg232Ter(p.R232*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript