RGD:11642226 Rat Genome Database

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Variant: RGD:11642226 -  Homo sapiens

RGD ID: 11642226
RS ID: rs200120991
ClinVar ID: CV269095
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HDAC4  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 2 240,033,214
GRCh38 2 239,111,518
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_009235.1:g.294430G>A
NC_000002.12:g.239111518C>T
NC_000002.11:g.240033214C>T
NM_001378416.1:c.1963+8G>A
More... 		12/07/2015 intron variant likely benign AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:HDAC4
Accession:XM_017005394
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_047446490
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_047446477
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_006712877
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_006712880
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_011512217
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_047446484
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_047446487
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_011512222
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_011512218
Location:INTRON

Gene Symbol:HDAC4
Accession:NM_001378415
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_047446488
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_047446483
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_011512224
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_011512227
Location:INTRON

Gene Symbol:HDAC4
Accession:NM_001378414
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_047446486
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_047446496
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_047446480
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_047446479
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_011512219
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_011512220
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_047446491
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_047446493
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_047446494
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_047446478
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_011512225
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_047446492
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_047446482
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_047446476
Location:INTRON

Gene Symbol:HDAC4
Accession:NM_001378417
Location:INTRON

Gene Symbol:HDAC4
Accession:NM_001378416
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_047446489
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_024453257
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_011512223
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_047446498
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_047446481
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_011512226
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_047446497
Location:INTRON

Gene Symbol:HDAC4
Accession:NM_006037
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_047446495
Location:INTRON

Gene Symbol:HDAC4
Accession:XM_047446485
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000371135 CLINVAR
dbSNP (RS) rs200120991 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene HDAC4 CLINVAR
OMIM 605314 CLINVAR