Primary Site >> Liver Cancer

Gene >> NHS

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000380060
Start 17728682:17728682(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4193C>T
AA Mutation p.Pro1398Leu(p.P1398L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000380060
Start 17725636:17725636(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1467A>G
Mutation Classification Silent
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000380060
Start 17727421:17727421(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3252T>C
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence frameshift_variant
Transcription ID ENST00000380060
Start 17692459:17692459(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.843delC
AA Mutation p.Leu283Ter(p.L283*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000380060
Start 17727049:17727049(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2880delA
AA Mutation p.Glu961ArgfsTer87(p.E961Rfs*87)
Mutation Classification Frame_Shift_Del
Feature Type Transcript