Primary Site >> Esophagus Cancer

Gene >> DIAPH2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000324765
Start 96918529:96918529(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.890C>A
AA Mutation p.Ala297Asp(p.A297D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000324765
Start 97247804:97247804(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763576938
CDS Mutation c.2809G>C
AA Mutation p.Glu937Gln(p.E937Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000324765
Start 96937270:96937270(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1127A>T
AA Mutation p.Gln376Leu(p.Q376L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000324765
Start 97141713:97141713(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2638A>G
AA Mutation p.Ile880Val(p.I880V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000324765
Start 97099740:97099740(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2294C>T
AA Mutation p.Ala765Val(p.A765V)
Mutation Classification Missense_Mutation
Feature Type Transcript