Primary Site >> Stomach Cancer

Gene >> NRN1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000244766
Start 5999055:5999055(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.350C>T
AA Mutation p.Ala117Val(p.A117V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000244766
Start 5999091:5999091(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.314G>T
AA Mutation p.Gly105Val(p.G105V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000244766
Start 5999146:5999146(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.259G>C
AA Mutation p.Ala87Pro(p.A87P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000244766
Start 6002469:6002469(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764429593
CDS Mutation c.84G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000244766
Start 6002415:6002415(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.138C>T
Mutation Classification Silent
Feature Type Transcript