Primary Site >> Stomach Cancer

Gene >> MAGED1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000326587
Start 51895650:51895650(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781817508
CDS Mutation c.643G>A
AA Mutation p.Asp215Asn(p.D215N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000326587
Start 51897591:51897591(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1531G>A
AA Mutation p.Glu511Lys(p.E511K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000326587
Start 51895536:51895536(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.529C>T
AA Mutation p.Pro177Ser(p.P177S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000326587
Start 51895590:51895590(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.583A>G
AA Mutation p.Thr195Ala(p.T195A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000326587
Start 51897209:51897209(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1424C>T
AA Mutation p.Ala475Val(p.A475V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000326587
Start 51895193:51895193(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.186G>A
AA Mutation p.Met62Ile(p.M62I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000326587
Start 51896502:51896502(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.847A>G
AA Mutation p.Thr283Ala(p.T283A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000326587
Start 51901671:51901671(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782675141
CDS Mutation c.2078G>A
AA Mutation p.Arg693His(p.R693H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000326587
Start 51896521:51896521(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.866G>A
AA Mutation p.Gly289Asp(p.G289D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000326587
Start 51895674:51895674(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.667G>T
AA Mutation p.Gly223Cys(p.G223C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000326587
Start 51896702:51896702(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1047C>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000326587
Start 51896600:51896600(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.945G>A
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000326587
Start 51900215:51900215(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1883delC
AA Mutation p.Pro628ArgfsTer18(p.P628Rfs*18)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence stop_gained
Transcription ID ENST00000326587
Start 51898295:51898295(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1749G>A
AA Mutation p.Trp583Ter(p.W583*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000326587
Start 51900214:51900215(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1883dupC
AA Mutation p.Glu629GlyfsTer3(p.E629Gfs*3)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript