Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PMCH

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000329406
Start 102197665:102197665(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.106G>A
AA Mutation p.Asp36Asn(p.D36N)
Mutation Classification Missense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> PMCH

No Mutation Annotation!