Primary Site >> Liver Cancer

Gene >> NAV3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000397909
Start 78119422:78119422(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3226T>G
AA Mutation p.Ser1076Ala(p.S1076A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000397909
Start 78128842:78128842(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4417G>A
AA Mutation p.Gly1473Arg(p.G1473R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000397909
Start 78058997:78058997(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2518T>C
AA Mutation p.Tyr840His(p.Y840H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000397909
Start 78185648:78185648(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5740C>A
AA Mutation p.Arg1914Ser(p.R1914S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000397909
Start 78159232:78159232(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4815C>A
AA Mutation p.Ser1605Arg(p.S1605R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000397909
Start 78119672:78119672(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3476C>G
AA Mutation p.Thr1159Ser(p.T1159S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000397909
Start 78006715:78006715(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1177G>A
AA Mutation p.Ala393Thr(p.A393T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000397909
Start 78119923:78119923(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3727A>G
AA Mutation p.Ile1243Val(p.I1243V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000397909
Start 78122035:78122035(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3845T>C
AA Mutation p.Leu1282Ser(p.L1282S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000397909
Start 77968635:77968635(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.604C>A
Mutation Classification Silent
Feature Type Transcript