Primary Site >> Stomach Cancer

Gene >> PSMA6

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261479
Start 35313033:35313033(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.562G>C
AA Mutation p.Asp188His(p.D188H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261479
Start 35312920:35312920(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.449A>G
AA Mutation p.Gln150Arg(p.Q150R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000261479
Start 35310770:35310770(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.284G>A
AA Mutation p.Arg95His(p.R95H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000261479
Start 35308960:35308960(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.218C>A
AA Mutation p.Thr73Asn(p.T73N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000261479
Start 35313010:35313010(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.546delA
AA Mutation p.Val183Ter(p.V183*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant;splice_region_variant
Transcription ID ENST00000261479
Start 35292552:35292553(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.76_76+1insAATATGCTTTTAA
AA Mutation p.Ala31IlefsTer4(p.A31Ifs*4)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript