Primary Site >> Stomach Cancer

Gene >> MBD2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000256429
Start 54164631:54164631(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201919549
CDS Mutation c.1001C>T
AA Mutation p.Ala334Val(p.A334V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000256429
Start 54159875:54159875(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1138C>T
AA Mutation p.Arg380Cys(p.R380C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000256429
Start 54224154:54224154(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.406C>T
AA Mutation p.Pro136Ser(p.P136S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000256429
Start 54164608:54164608(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs182260595
CDS Mutation c.1024G>A
AA Mutation p.Ala342Thr(p.A342T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000256429
Start 54164655:54164655(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.977C>T
AA Mutation p.Ala326Val(p.A326V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000256429
Start 54224089:54224089(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs755716804
CDS Mutation c.471delC
AA Mutation p.Gly158AspfsTer7(p.G158Dfs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 7
Mutation Consequence stop_gained
Transcription ID ENST00000256429
Start 54205024:54205024(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.676C>T
AA Mutation p.Arg226Ter(p.R226*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript