Primary Site >> Stomach Cancer

Gene >> F2R

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000319211
Start 76733278:76733278(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1053T>A
AA Mutation p.Phe351Leu(p.F351L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000319211
Start 76732752:76732752(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.527G>C
AA Mutation p.Arg176Pro(p.R176P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000319211
Start 76733229:76733229(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs17849599
CDS Mutation c.1004C>T
AA Mutation p.Ala335Val(p.A335V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000319211
Start 76733499:76733499(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1274C>T
AA Mutation p.Thr425Ile(p.T425I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000319211
Start 76733085:76733085(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771205478
CDS Mutation c.860C>T
AA Mutation p.Thr287Met(p.T287M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000319211
Start 76732899:76732899(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.674C>T
AA Mutation p.Ala225Val(p.A225V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000319211
Start 76732624:76732624(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.399C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000319211
Start 76733344:76733344(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1119C>T
Mutation Classification Silent
Feature Type Transcript