Primary Site >> Liver Cancer

Gene >> HIPK3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000303296
Start 33286964:33286964(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.550T>A
AA Mutation p.Leu184Ile(p.L184I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000303296
Start 33328547:33328547(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1135G>A
AA Mutation p.Ala379Thr(p.A379T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000303296
Start 33286694:33286694(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.280G>A
AA Mutation p.Val94Ile(p.V94I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000303296
Start 33287378:33287378(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.964G>T
AA Mutation p.Asp322Tyr(p.D322Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000303296
Start 33337170:33337170(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1317G>T
AA Mutation p.Met439Ile(p.M439I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000303296
Start 33337158:33337158(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1305A>T
AA Mutation p.Lys435Asn(p.K435N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000303296
Start 33337160:33337160(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1307A>C
AA Mutation p.Glu436Ala(p.E436A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000303296
Start 33287476:33287476(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1062T>C
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000303296
Start 33353096:33353127(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.3176_3207delAGCACTTTGGATCTGGGCATCAAGAGTGGAAT
AA Mutation p.Gln1059ArgfsTer15(p.Q1059Rfs*15)
Mutation Classification Frame_Shift_Del
Feature Type Transcript