Primary Site >> Liver Cancer

Gene >> NOX4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000263317
Start 89440705:89440705(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.458A>T
AA Mutation p.Lys153Ile(p.K153I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000263317
Start 89335921:89335921(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1540G>C
AA Mutation p.Ala514Pro(p.A514P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000263317
Start 89449506:89449506(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.283A>T
AA Mutation p.Arg95Trp(p.R95W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000263317
Start 89400061:89400061(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1030C>G
AA Mutation p.Pro344Ala(p.P344A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000263317
Start 89335938:89335938(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1523T>G
AA Mutation p.Ile508Ser(p.I508S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000263317
Start 89335886:89335886(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1575G>C
Mutation Classification Silent
Feature Type Transcript