Primary Site >> Liver Cancer

Gene >> PCDH9

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000377865
Start 67225426:67225426(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3015G>T
AA Mutation p.Lys1005Asn(p.K1005N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000377865
Start 66631216:66631216(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3334A>G
AA Mutation p.Asn1112Asp(p.N1112D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000377865
Start 66304759:66304759(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760160903
CDS Mutation c.3610C>T
AA Mutation p.His1204Tyr(p.H1204Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000377865
Start 67226817:67226817(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1624G>A
AA Mutation p.Val542Ile(p.V542I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000377865
Start 67226831:67226831(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1610G>A
AA Mutation p.Arg537Gln(p.R537Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000377865
Start 67225821:67225821(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2620A>G
AA Mutation p.Arg874Gly(p.R874G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000377865
Start 66304899:66304899(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3470C>T
AA Mutation p.Pro1157Leu(p.P1157L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000377865
Start 66304880:66304880(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3489C>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000377865
Start 67227231:67227231(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1210G>T
AA Mutation p.Glu404Ter(p.E404*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000377865
Start 67226978:67226978(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1463T>A
AA Mutation p.Leu488Ter(p.L488*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript