Primary Site >> Esophagus Cancer

Gene >> MAGED1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000326587
Start 51896658:51896658(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1003C>T
AA Mutation p.Pro335Ser(p.P335S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000326587
Start 51901886:51901886(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2293T>G
AA Mutation p.Phe765Val(p.F765V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000326587
Start 51901795:51901795(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2202C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence inframe_deletion
Transcription ID ENST00000326587
Start 51896649:51896666(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1008_1025delCGCTTGGCAGAACCCAGT
AA Mutation p.Ala337_Val342del(p.A337_V342del)
Mutation Classification In_Frame_Del
Feature Type Transcript