Primary Site >> Liver Cancer

Gene >> HDAC9

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18727730:18727730(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1873C>A
AA Mutation p.Arg625Ser(p.R625S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000432645
Start 18762277:18762277(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2155G>T
AA Mutation p.Gly719Cys(p.G719C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18648676:18648676(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1451T>A
AA Mutation p.Met484Lys(p.M484K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18829472:18829472(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2381T>A
AA Mutation p.Phe794Tyr(p.F794Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18647861:18647861(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1103A>G
AA Mutation p.Tyr368Cys(p.Y368C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18585340:18585340(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.82A>T
AA Mutation p.Thr28Ser(p.T28S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000432645
Start 18666328:18666328(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1574A>G
AA Mutation p.Asn525Ser(p.N525S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000432645
Start 18647944:18647944(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1186C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000432645
Start 18648497:18648497(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1272G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence splice_donor_variant
Transcription ID ENST00000432645
Start 18793453:18793453(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2313+1G>A
Mutation Classification Splice_Site
Feature Type Transcript