RGD:14727766 Rat Genome Database

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Variant: RGD:14727766 -  Homo sapiens

RGD ID: 14727766
RS ID: rs781824575
ClinVar ID: CV671177
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HDAC8  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 X 71,792,461
GRCh38 X 72,572,611
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001166418.2:c.111+40T>G
NM_001166419.2:c.111+40T>G
NM_001166422.2:c.111+40T>G
NM_001166448.2:c.111+40T>G
More... 		06/16/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:HDAC8
Accession:XM_017029640
Location:INTRON

Gene Symbol:HDAC8
Accession:NM_001166422
Location:INTRON

Gene Symbol:HDAC8
Accession:XM_047442255
Location:INTRON

Gene Symbol:HDAC8
Accession:XM_047442257
Location:INTRON

Gene Symbol:HDAC8
Accession:NM_001410728
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:HDAC8
Accession:XM_047442252
Location:INTRON

Gene Symbol:HDAC8
Accession:NM_001166419
Location:INTRON

Gene Symbol:HDAC8
Accession:XM_017029644
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:HDAC8
Accession:XM_047442256
Location:INTRON

Gene Symbol:HDAC8
Accession:NM_018486
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:HDAC8
Accession:XM_017029643
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:HDAC8
Accession:NM_001166448
Location:INTRON

Gene Symbol:HDAC8
Accession:NM_001410725
Location:INTRON

Gene Symbol:HDAC8
Accession:NM_001410727
Location:INTRON

Gene Symbol:HDAC8
Accession:NM_001410730
Location:INTRON

Gene Symbol:HDAC8
Accession:NM_001166418
Location:INTRON

Gene Symbol:HDAC8
Accession:XM_017029645
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:HDAC8
Accession:NM_001166420
Location:INTRON

Gene Symbol:HDAC8
Accession:NM_001410729
Location:INTRON

Gene Symbol:HDAC8
Accession:NR_051952
Location:INTRON;NON-CODING

Gene Symbol:HDAC8
Accession:XR_938402
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000834471 CLINVAR
dbSNP (RS) rs781824575 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene HDAC8 CLINVAR
OMIM 300269 CLINVAR