Primary Site >> Esophagus Cancer

Gene >> AXIN2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000307078
Start 65535670:65535670(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2193G>T
AA Mutation p.Gln731His(p.Q731H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000307078
Start 65535682:65535682(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2181G>A
Mutation Classification Silent
Feature Type Transcript