Primary Site >> Stomach Cancer

Gene >> RFC3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000380071
Start 33835209:33835209(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.871A>G
AA Mutation p.Ile291Val(p.I291V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000380071
Start 33835161:33835161(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761845498
CDS Mutation c.823C>T
AA Mutation p.Arg275Cys(p.R275C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000380071
Start 33836227:33836227(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1003T>C
AA Mutation p.Phe335Leu(p.F335L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000380071
Start 33829893:33829893(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.449G>A
AA Mutation p.Arg150Lys(p.R150K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000380071
Start 33829993:33829993(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.549T>G
Mutation Classification Silent
Feature Type Transcript