Primary Site >> Esophagus Cancer

Gene >> ANO2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000356134
Start 5565613:5565613(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767967144
CDS Mutation c.2675C>T
AA Mutation p.Ser892Leu(p.S892L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000356134
Start 5732596:5732596(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1472G>C
AA Mutation p.Arg491Pro(p.R491P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000356134
Start 5563458:5563458(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2841G>C
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000356134
Start 5578432:5578432(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2323C>A
Mutation Classification Silent
Feature Type Transcript