Primary Site >> Stomach Cancer

Gene >> GP9

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000307395
Start 129061835:129061835(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.96G>T
AA Mutation p.Met32Ile(p.M32I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000307395
Start 129061922:129061922(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.183C>G
AA Mutation p.Asn61Lys(p.N61K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000307395
Start 129062014:129062014(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.275G>A
AA Mutation p.Ser92Asn(p.S92N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000307395
Start 129062064:129062064(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.325C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000307395
Start 129061853:129061853(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.114C>T
Mutation Classification Silent
Feature Type Transcript