Primary Site >> Stomach Cancer

Gene >> MXD1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264444
Start 69937251:69937251(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.335A>G
AA Mutation p.Asp112Gly(p.D112G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264444
Start 69938105:69938105(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs535119144
CDS Mutation c.487G>A
AA Mutation p.Asp163Asn(p.D163N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000264444
Start 69916160:69916160(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.113A>G
AA Mutation p.Asn38Ser(p.N38S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000264444
Start 69935430:69935430(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.283T>C
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000264444
Start 69937273:69937273(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs141349752
CDS Mutation c.357C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence stop_gained
Transcription ID ENST00000264444
Start 69937277:69937277(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.361C>T
AA Mutation p.Gln121Ter(p.Q121*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence stop_gained
Transcription ID ENST00000264444
Start 69935418:69935418(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.271C>T
AA Mutation p.Arg91Ter(p.R91*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript