Primary Site >> Stomach Cancer

Gene >> RNF34

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000361234
Start 121417718:121417718(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.440T>C
AA Mutation p.Val147Ala(p.V147A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000361234
Start 121416357:121416357(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.205T>G
AA Mutation p.Phe69Val(p.F69V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000361234
Start 121416316:121416316(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.164C>T
AA Mutation p.Thr55Met(p.T55M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000361234
Start 121423505:121423505(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1048G>A
AA Mutation p.Gly350Ser(p.G350S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000361234
Start 121420289:121420289(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377017432
CDS Mutation c.681C>T
Mutation Classification Silent
Feature Type Transcript