Primary Site >> Esophagus Cancer

Gene >> MAMLD1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000262858
Start 150471067:150471067(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1494G>T
AA Mutation p.Gln498His(p.Q498H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000262858
Start 150470564:150470564(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.991C>G
AA Mutation p.Leu331Val(p.L331V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000262858
Start 150470612:150470612(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1039C>A
AA Mutation p.His347Asn(p.H347N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000262858
Start 150470977:150470977(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1404G>T
AA Mutation p.Leu468Phe(p.L468F)
Mutation Classification Missense_Mutation
Feature Type Transcript