Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TSPAN33

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000486685
Start 129167861:129167861(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.839A>G
AA Mutation p.Asp280Gly(p.D280G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000486685
Start 129167826:129167826(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.804C>G
AA Mutation p.Ile268Met(p.I268M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000486685
Start 129164556:129164556(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.446T>G
AA Mutation p.Phe149Cys(p.F149C)
Mutation Classification Missense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> TSPAN33

No Mutation Annotation!