Primary Site >> Esophagus Cancer

Gene >> SLC39A7

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000374675
Start 33203032:33203032(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1063G>A
AA Mutation p.Val355Ile(p.V355I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000374675
Start 33201865:33201865(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.532G>A
AA Mutation p.Gly178Ser(p.G178S)
Mutation Classification Missense_Mutation
Feature Type Transcript