Primary Site >> Liver Cancer

Gene >> HHAT

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261458
Start 210464540:210464540(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.892G>T
AA Mutation p.Val298Leu(p.V298L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261458
Start 210674302:210674302(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1405A>T
AA Mutation p.Thr469Ser(p.T469S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000261458
Start 210418283:210418283(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.814A>T
AA Mutation p.Ser272Cys(p.S272C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000261458
Start 210464606:210464606(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143700139
CDS Mutation c.958G>A
AA Mutation p.Ala320Thr(p.A320T)
Mutation Classification Missense_Mutation
Feature Type Transcript