Primary Site >> Stomach Cancer

Gene >> MBD4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000249910
Start 129436677:129436677(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.967T>G
AA Mutation p.Phe323Val(p.F323V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000249910
Start 129437294:129437294(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757487617
CDS Mutation c.350A>C
AA Mutation p.Lys117Thr(p.K117T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000249910
Start 129433943:129433943(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1318C>A
AA Mutation p.Pro440Thr(p.P440T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000249910
Start 129437873:129437873(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.182G>A
AA Mutation p.Cys61Tyr(p.C61Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000249910
Start 129437868:129437868(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.187C>T
AA Mutation p.Pro63Ser(p.P63S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000249910
Start 129434093:129434093(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1245C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000249910
Start 129436705:129436706(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.938_939delAA
AA Mutation p.Lys313ArgfsTer13(p.K313Rfs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript