Primary Site >> Liver Cancer

Gene >> NPTX2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000265634
Start 98628618:98628618(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1285C>T
AA Mutation p.Leu429Phe(p.L429F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000265634
Start 98624952:98624952(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.674T>C
AA Mutation p.Phe225Ser(p.F225S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000265634
Start 98627196:98627196(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.920G>T
AA Mutation p.Gly307Val(p.G307V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000265634
Start 98625079:98625079(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779765826
CDS Mutation c.801C>G
Mutation Classification Silent
Feature Type Transcript