Primary Site >> Liver Cancer

Gene >> TLE4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000376552
Start 79718922:79718922(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1541A>T
AA Mutation p.Asp514Val(p.D514V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000376552
Start 79652626:79652626(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.424C>A
AA Mutation p.His142Asn(p.H142N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000376552
Start 79718812:79718812(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1431T>A
AA Mutation p.His477Gln(p.H477Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000376552
Start 79705921:79705921(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.762G>T
AA Mutation p.Leu254Phe(p.L254F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000376552
Start 79705922:79705922(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.763G>T
AA Mutation p.Val255Leu(p.V255L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000376552
Start 79709636:79709636(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1277C>G
AA Mutation p.Pro426Arg(p.P426R)
Mutation Classification Missense_Mutation
Feature Type Transcript