Primary Site >> Liver Cancer

Gene >> CLCA1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000234701
Start 86493485:86493485(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1566G>T
AA Mutation p.Trp522Cys(p.W522C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000234701
Start 86495624:86495624(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2062G>T
AA Mutation p.Val688Leu(p.V688L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000234701
Start 86499874:86499874(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2574C>A
AA Mutation p.Asn858Lys(p.N858K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000234701
Start 86499875:86499875(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2575A>G
AA Mutation p.Ile859Val(p.I859V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000234701
Start 86473831:86473831(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.406C>A
AA Mutation p.Pro136Thr(p.P136T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000234701
Start 86494386:86494386(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1880C>A
AA Mutation p.Thr627Lys(p.T627K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000234701
Start 86498740:86498740(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2282C>T
AA Mutation p.Ala761Val(p.A761V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000234701
Start 86482335:86482335(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.688C>A
AA Mutation p.Arg230Ser(p.R230S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000234701
Start 86489130:86489130(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1317C>T
Mutation Classification Silent
Feature Type Transcript