Primary Site >> Pancreatic Cancer

Gene >> MATK

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000310132
Start 3783845:3783845(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.551T>C
AA Mutation p.Val184Ala(p.V184A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000310132
Start 3784222:3784222(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.264C>T
Mutation Classification Silent
Feature Type Transcript