Primary Site >> Liver Cancer

Gene >> HK2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000290573
Start 74886508:74886508(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2054G>T
AA Mutation p.Cys685Phe(p.C685F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000290573
Start 74880281:74880281(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1282C>G
AA Mutation p.His428Asp(p.H428D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000290573
Start 74886654:74886654(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2200C>T
AA Mutation p.Leu734Phe(p.L734F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000290573
Start 74854327:74854327(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.98A>G
AA Mutation p.Asp33Gly(p.D33G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000290573
Start 74882236:74882236(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200225889
CDS Mutation c.1836C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000290573
Start 74877241:74877241(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.951G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000290573
Start 74886365:74886365(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2007C>T
Mutation Classification Silent
Feature Type Transcript