Primary Site >> Stomach Cancer

Gene >> AMPD1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000520113
Start 114688699:114688699(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.176C>T
AA Mutation p.Ala59Val(p.A59V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000520113
Start 114675947:114675947(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1544T>A
AA Mutation p.Ile515Asn(p.I515N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000520113
Start 114686903:114686903(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs12566550
CDS Mutation c.322C>T
AA Mutation p.Arg108Cys(p.R108C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000520113
Start 114677478:114677478(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1360C>T
AA Mutation p.His454Tyr(p.H454Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000520113
Start 114673683:114673683(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374697989
CDS Mutation c.2140G>A
AA Mutation p.Glu714Lys(p.E714K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000520113
Start 114675598:114675598(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1710G>T
AA Mutation p.Lys570Asn(p.K570N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000520113
Start 114684282:114684282(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.563T>G
AA Mutation p.Phe188Cys(p.F188C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000520113
Start 114676000:114676000(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1491T>G
AA Mutation p.Asp497Glu(p.D497E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000520113
Start 114675986:114675986(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1505A>C
AA Mutation p.Lys502Thr(p.K502T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000520113
Start 114674813:114674813(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1838C>T
AA Mutation p.Thr613Ile(p.T613I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000520113
Start 114675575:114675575(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1733C>T
AA Mutation p.Ala578Val(p.A578V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000520113
Start 114678453:114678453(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1071A>G
Mutation Classification Silent
Feature Type Transcript