Primary Site >> Stomach Cancer

Gene >> PLK3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000372201
Start 44805616:44805616(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1879C>T
AA Mutation p.Pro627Ser(p.P627S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000372201
Start 44804444:44804444(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779691195
CDS Mutation c.1448G>A
AA Mutation p.Arg483His(p.R483H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000372201
Start 44800870:44800870(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.241G>A
AA Mutation p.Asp81Asn(p.D81N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000372201
Start 44803126:44803126(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.921G>T
AA Mutation p.Gln307His(p.Q307H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000372201
Start 44805665:44805665(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776334966
CDS Mutation c.1928G>A
AA Mutation p.Arg643His(p.R643H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000372201
Start 44801902:44801902(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.623C>T
AA Mutation p.Ala208Val(p.A208V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000372201
Start 44804490:44804490(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1494G>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000372201
Start 44803325:44803325(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1011delC
AA Mutation p.Asn338ThrfsTer35(p.N338Tfs*35)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000372201
Start 44804354:44804354(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1363delC
AA Mutation p.Leu455TrpfsTer90(p.L455Wfs*90)
Mutation Classification Frame_Shift_Del
Feature Type Transcript