Primary Site >> Stomach Cancer

Gene >> OLR1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000309539
Start 10166880:10166880(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.256T>C
AA Mutation p.Ser86Pro(p.S86P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000309539
Start 10169112:10169112(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.140T>C
AA Mutation p.Leu47Pro(p.L47P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000309539
Start 10160459:10160459(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.568T>G
AA Mutation p.Phe190Val(p.F190V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000309539
Start 10160823:10160823(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.527A>T
AA Mutation p.Asp176Val(p.D176V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000309539
Start 10172033:10172033(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.45T>C
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000309539
Start 10159925:10159925(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.777T>C
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence splice_donor_variant
Transcription ID ENST00000309539
Start 10169072:10169072(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.178+2T>C
Mutation Classification Splice_Site
Feature Type Transcript