Primary Site >> Stomach Cancer

Gene >> OR13C8

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000335040
Start 104569632:104569632(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.465C>A
AA Mutation p.Asp155Glu(p.D155E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000335040
Start 104569601:104569601(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.434C>T
AA Mutation p.Ala145Val(p.A145V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000335040
Start 104569464:104569464(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs543122936
CDS Mutation c.297G>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000335040
Start 104569524:104569524(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.357A>G
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence stop_lost
Transcription ID ENST00000335040
Start 104570128:104570128(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.961T>G
AA Mutation p.Ter321GlyextTer?(p.*321Gext*?)
Mutation Classification Nonstop_Mutation
Feature Type Transcript