Primary Site >> Stomach Cancer

Gene >> PPM1A

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000395076
Start 60282801:60282801(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.98G>A
AA Mutation p.Arg33His(p.R33H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000395076
Start 60283235:60283235(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.532G>A
AA Mutation p.Ala178Thr(p.A178T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000395076
Start 60289830:60289830(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755646949
CDS Mutation c.977G>A
AA Mutation p.Gly326Asp(p.G326D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000395076
Start 60283029:60283029(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.326A>G
AA Mutation p.Asp109Gly(p.D109G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000395076
Start 60289856:60289856(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1003C>T
AA Mutation p.Arg335Cys(p.R335C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000395076
Start 60291415:60291415(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1080C>T
Mutation Classification Silent
Feature Type Transcript