Primary Site >> Liver Cancer

Gene >> DOCK8

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000432829
Start 434955:434955(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767895149
CDS Mutation c.5059G>A
AA Mutation p.Val1687Met(p.V1687M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000432829
Start 368060:368060(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1722C>A
AA Mutation p.Asn574Lys(p.N574K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000432829
Start 429834:429834(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4606T>C
AA Mutation p.Phe1536Leu(p.F1536L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000432829
Start 396809:396809(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745843220
CDS Mutation c.2995C>G
AA Mutation p.His999Asp(p.H999D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000432829
Start 434898:434898(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759524696
CDS Mutation c.5002G>A
AA Mutation p.Ala1668Thr(p.A1668T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000432829
Start 446496:446496(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5707G>T
AA Mutation p.Gly1903Trp(p.G1903W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000432829
Start 328171:328171(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1044G>C
AA Mutation p.Lys348Asn(p.K348N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000432829
Start 396879:396879(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3065C>T
AA Mutation p.Thr1022Ile(p.T1022I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000432829
Start 371468:371468(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1909G>T
AA Mutation p.Ala637Ser(p.A637S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000432829
Start 439312:439312(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5147G>T
AA Mutation p.Gly1716Val(p.G1716V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000432829
Start 376287:376287(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2187T>C
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000432829
Start 336700:336700(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1404T>A
Mutation Classification Silent
Feature Type Transcript