Primary Site >> Esophagus Cancer

Gene >> HSPH1

ID 1
Mutation Consequence synonymous_variant
Transcription ID ENST00000320027
Start 31147990:31147990(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1347C>A
Mutation Classification Silent
Feature Type Transcript
ID 2
Mutation Consequence frameshift_variant
Transcription ID ENST00000320027
Start 31155532:31155533(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.287dupA
AA Mutation p.Asn96LysfsTer13(p.N96Kfs*13)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript