Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FAM162A

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000477892
Start 122409818:122409818(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.452C>T
AA Mutation p.Ala151Val(p.A151V)
Mutation Classification Missense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> FAM162A

No Mutation Annotation!