Primary Site >> Liver Cancer

Gene >> HUWE1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000262854
Start 53547748:53547748(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.10561A>G
AA Mutation p.Thr3521Ala(p.T3521A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000262854
Start 53536200:53536200(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.12478C>G
AA Mutation p.Leu4160Val(p.L4160V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000262854
Start 53628761:53628761(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1105G>A
AA Mutation p.Ala369Thr(p.A369T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000262854
Start 53534538:53534538(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.12809A>T
AA Mutation p.Lys4270Met(p.K4270M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000262854
Start 53592483:53592483(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3887A>T
AA Mutation p.Glu1296Val(p.E1296V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000262854
Start 53576912:53576912(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5872G>A
AA Mutation p.Ala1958Thr(p.A1958T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000262854
Start 53552441:53552441(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8751C>A
AA Mutation p.Ser2917Arg(p.S2917R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000262854
Start 53590417:53590417(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4178C>T
AA Mutation p.Ala1393Val(p.A1393V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000262854
Start 53645429:53645429(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.386A>T
AA Mutation p.Gln129Leu(p.Q129L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000262854
Start 53551136:53551136(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9150C>A
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000262854
Start 53564688:53564688(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6915T>C
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000262854
Start 53552766:53552766(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8622T>A
Mutation Classification Silent
Feature Type Transcript