Primary Site >> Stomach Cancer

Gene >> RPRM

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000325926
Start 153478481:153478481(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.85T>C
AA Mutation p.Cys29Arg(p.C29R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000325926
Start 153478376:153478376(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.190G>A
AA Mutation p.Val64Met(p.V64M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000325926
Start 153478505:153478505(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.61G>A
AA Mutation p.Glu21Lys(p.E21K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000325926
Start 153478421:153478421(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.145C>T
AA Mutation p.Arg49Cys(p.R49C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000325926
Start 153478363:153478363(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.203C>T
AA Mutation p.Thr68Ile(p.T68I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000325926
Start 153478429:153478429(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.137C>T
AA Mutation p.Pro46Leu(p.P46L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000325926
Start 153478328:153478328(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.238C>T
Mutation Classification Silent
Feature Type Transcript