Primary Site >> Stomach Cancer

Gene >> MX2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000330714
Start 41399223:41399223(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745448850
CDS Mutation c.1300G>A
AA Mutation p.Glu434Lys(p.E434K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000330714
Start 41399001:41399001(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1254G>T
AA Mutation p.Lys418Asn(p.K418N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000330714
Start 41408190:41408190(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs548863071
CDS Mutation c.2105C>T
AA Mutation p.Ala702Val(p.A702V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000330714
Start 41390658:41390658(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.826C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000330714
Start 41398902:41398902(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201893416
CDS Mutation c.1155G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000330714
Start 41408194:41408194(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2109A>G
Mutation Classification Silent
Feature Type Transcript