Primary Site >> Liver Cancer

Gene >> KNTC1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000333479
Start 122601552:122601552(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4580A>G
AA Mutation p.Tyr1527Cys(p.Y1527C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000333479
Start 122573167:122573167(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2165G>C
AA Mutation p.Arg722Pro(p.R722P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000333479
Start 122585715:122585715(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3614A>T
AA Mutation p.Glu1205Val(p.E1205V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000333479
Start 122571060:122571060(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1953G>C
AA Mutation p.Glu651Asp(p.E651D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000333479
Start 122621879:122621879(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6280-2A>T
Mutation Classification Splice_Site
Feature Type Transcript
ID 6
Mutation Consequence splice_acceptor_variant;coding_sequence_variant;intron_variant
Transcription ID ENST00000333479
Start 122570870:122570882(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1861-4_1869delTCAGATAATTCTT
Mutation Classification Splice_Site
Feature Type Transcript