Primary Site >> Stomach Cancer

Gene >> NCR1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000291890
Start 54910059:54910059(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.676T>G
AA Mutation p.Phe226Val(p.F226V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000291890
Start 54910050:54910050(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.667G>A
AA Mutation p.Asp223Asn(p.D223N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000291890
Start 54909393:54909393(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765774550
CDS Mutation c.504C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000291890
Start 54906217:54906217(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371994983
CDS Mutation c.30C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence stop_gained
Transcription ID ENST00000291890
Start 54909454:54909454(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.565C>T
AA Mutation p.Arg189Ter(p.R189*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript