Primary Site >> Stomach Cancer

Gene >> SLC18A1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000276373
Start 20179419:20179419(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750496793
CDS Mutation c.190G>A
AA Mutation p.Gly64Ser(p.G64S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000276373
Start 20150666:20150666(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747952915
CDS Mutation c.1094G>T
AA Mutation p.Arg365Leu(p.R365L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000276373
Start 20149708:20149708(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759912369
CDS Mutation c.1114G>A
AA Mutation p.Gly372Arg(p.G372R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000276373
Start 20165099:20165099(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.867G>T
AA Mutation p.Lys289Asn(p.K289N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000276373
Start 20179374:20179374(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.235T>G
AA Mutation p.Ser79Ala(p.S79A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000276373
Start 20147283:20147283(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1439G>A
AA Mutation p.Ser480Asn(p.S480N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000276373
Start 20150687:20150687(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1073T>C
AA Mutation p.Val358Ala(p.V358A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000276373
Start 20150689:20150689(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1071T>C
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000276373
Start 20147277:20147277(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1445delC
AA Mutation p.Pro482ArgfsTer10(p.P482Rfs*10)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000276373
Start 20179387:20179388(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.221_222delCC
AA Mutation p.Ala74ValfsTer19(p.A74Vfs*19)
Mutation Classification Frame_Shift_Del
Feature Type Transcript