Primary Site >> Liver Cancer

Gene >> KIAA1210

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000402510
Start 119089471:119089471(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1759T>A
AA Mutation p.Leu587Met(p.L587M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000402510
Start 119089000:119089000(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2230A>T
AA Mutation p.Ser744Cys(p.S744C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000402510
Start 119086879:119086879(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4351G>A
AA Mutation p.Glu1451Lys(p.E1451K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000402510
Start 119147545:119147545(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781323631
CDS Mutation c.338A>G
AA Mutation p.Asp113Gly(p.D113G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000402510
Start 119096647:119096647(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1113G>T
AA Mutation p.Leu371Phe(p.L371F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000402510
Start 119096619:119096619(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1141A>T
AA Mutation p.Ser381Cys(p.S381C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000402510
Start 119116560:119116560(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.586T>C
AA Mutation p.Ser196Pro(p.S196P)
Mutation Classification Missense_Mutation
Feature Type Transcript