Primary Site >> Liver Cancer

Gene >> NOTCH4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000375023
Start 32196038:32196038(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5411C>T
AA Mutation p.Ala1804Val(p.A1804V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000375023
Start 32202308:32202308(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3523G>T
AA Mutation p.Ala1175Ser(p.A1175S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000375023
Start 32215337:32215337(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1910A>C
AA Mutation p.Lys637Thr(p.K637T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000375023
Start 32222628:32222628(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765988217
CDS Mutation c.334G>A
AA Mutation p.Glu112Lys(p.E112K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000375023
Start 32213694:32213694(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2314G>T
AA Mutation p.Val772Leu(p.V772L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000375023
Start 32214224:32214224(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2053G>T
AA Mutation p.Gly685Trp(p.G685W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000375023
Start 32196008:32196008(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5441A>G
AA Mutation p.Asp1814Gly(p.D1814G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000375023
Start 32199038:32199038(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4423C>T
AA Mutation p.Arg1475Cys(p.R1475C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000375023
Start 32220514:32220514(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1050A>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000375023
Start 32198497:32198497(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4680G>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000375023
Start 32212629:32212629(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2527-2A>T
Mutation Classification Splice_Site
Feature Type Transcript