Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SNAI1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000244050
Start 49987988:49987988(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.727C>T
AA Mutation p.Arg243Trp(p.R243W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000244050
Start 49984300:49984300(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.559A>G
AA Mutation p.Lys187Glu(p.K187E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000244050
Start 49987874:49987874(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.613G>A
AA Mutation p.Glu205Lys(p.E205K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000244050
Start 49987920:49987920(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.659G>A
AA Mutation p.Arg220His(p.R220H)
Mutation Classification Missense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> SNAI1

Mutation ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000244050
Start 49987874:49987874(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.613G>A
AA Mutation p.Glu205Lys(p.E205K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence start_lost
Transcription ID ENST00000244050
Start 49983061:49983061(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2T>C
AA Mutation p.Met1?(p.M1?)
Mutation Classification Translation_Start_Site
Feature Type Transcript