Primary Site >> Stomach Cancer

Gene >> PPP4C

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000279387
Start 30084722:30084722(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.661G>A
AA Mutation p.Val221Met(p.V221M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000279387
Start 30083512:30083512(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372333615
CDS Mutation c.422G>A
AA Mutation p.Arg141His(p.R141H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000279387
Start 30084967:30084967(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.829G>A
AA Mutation p.Glu277Lys(p.E277K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000279387
Start 30084732:30084732(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.671A>G
AA Mutation p.Gln224Arg(p.Q224R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000279387
Start 30084682:30084682(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.621C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000279387
Start 30084963:30084963(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.825G>A
Mutation Classification Silent
Feature Type Transcript