Primary Site >> Liver Cancer

Gene >> PKD1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000262304
Start 2111187:2111187(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3980A>C
AA Mutation p.Asp1327Ala(p.D1327A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000262304
Start 2108623:2108623(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6544C>G
AA Mutation p.Gln2182Glu(p.Q2182E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000262304
Start 2090512:2090512(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.12217A>G
AA Mutation p.Thr4073Ala(p.T4073A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000262304
Start 2099931:2099931(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201780393
CDS Mutation c.9853G>A
AA Mutation p.Val3285Ile(p.V3285I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000262304
Start 2099978:2099978(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9806G>T
AA Mutation p.Arg3269Leu(p.R3269L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000262304
Start 2108257:2108257(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6910A>G
AA Mutation p.Thr2304Ala(p.T2304A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000262304
Start 2092997:2092997(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.11113A>T
AA Mutation p.Ile3705Phe(p.I3705F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000262304
Start 2091434:2091434(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.11701C>T
Mutation Classification Silent
Feature Type Transcript