Primary Site >> Stomach Cancer

Gene >> OGFR

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000290291
Start 62809647:62809647(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.382C>T
AA Mutation p.His128Tyr(p.H128Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000290291
Start 62809614:62809614(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.349T>C
AA Mutation p.Trp117Arg(p.W117R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000290291
Start 62812561:62812561(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.946C>A
AA Mutation p.Pro316Thr(p.P316T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000290291
Start 62812884:62812884(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775575581
CDS Mutation c.1269C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000290291
Start 62810562:62810562(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768880230
CDS Mutation c.462C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000290291
Start 62812509:62812509(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.894C>T
Mutation Classification Silent
Feature Type Transcript