Primary Site >> Esophagus Cancer

Gene >> PRRX1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000239461
Start 170719824:170719824(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.340G>C
AA Mutation p.Glu114Gln(p.E114Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000239461
Start 170736121:170736121(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.673G>C
AA Mutation p.Ala225Pro(p.A225P)
Mutation Classification Missense_Mutation
Feature Type Transcript