Primary Site >> Liver Cancer

Gene >> LCK

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000336890
Start 32276355:32276355(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.650G>A
AA Mutation p.Cys217Tyr(p.C217Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000336890
Start 32276748:32276748(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.926A>T
AA Mutation p.Gln309Leu(p.Q309L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000336890
Start 32276054:32276054(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.622C>A
AA Mutation p.His208Asn(p.H208N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000336890
Start 32274405:32274405(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.76C>G
AA Mutation p.Pro26Ala(p.P26A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000336890
Start 32276053:32276053(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.621C>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000336890
Start 32275636:32275637(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.445_446insTGTGGATGCCTCTGTGGAGGTGGGATAGGGGGTGCCTCTGTGTGTGTGT
AA Mutation p.Gly149ValfsTer53(p.G149Vfs*53)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript