Primary Site >> Pancreatic Cancer

Gene >> HMMR

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000358715
Start 163464732:163464732(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.155A>T
AA Mutation p.Gln52Leu(p.Q52L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000358715
Start 163474187:163474187(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1032A>T
Mutation Classification Silent
Feature Type Transcript