Primary Site >> Stomach Cancer

Gene >> PPP1R12A

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261207
Start 79820900:79820900(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.988A>C
AA Mutation p.Asn330His(p.N330H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261207
Start 79809826:79809826(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1424G>A
AA Mutation p.Arg475Lys(p.R475K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000261207
Start 79793916:79793916(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2596G>A
AA Mutation p.Glu866Lys(p.E866K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000261207
Start 79817486:79817486(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1147G>A
AA Mutation p.Ala383Thr(p.A383T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000261207
Start 79820787:79820787(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1101A>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000261207
Start 79796810:79796810(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2433C>T
Mutation Classification Silent
Feature Type Transcript