Primary Site >> Liver Cancer

Gene >> NCAM1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113271779:113271779(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2359C>A
AA Mutation p.Pro787Thr(p.P787T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113207906:113207906(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782790715
CDS Mutation c.820A>G
AA Mutation p.Ile274Val(p.I274V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113233162:113233162(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1538C>T
AA Mutation p.Pro513Leu(p.P513L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113207870:113207870(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.784A>G
AA Mutation p.Lys262Glu(p.K262E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000316851
Start 113214484:113214484(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1032T>A
Mutation Classification Silent
Feature Type Transcript