RGD:401912588 Rat Genome Database

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Variant: RGD:401912588 -  Homo sapiens

RGD ID: 401912588
ClinVar ID: CV2824938
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DNAJC13  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 132,196,983
GRCh38 3 132,478,139
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NC_000003.11:g.132196983G>A
NP_056083.3:p.Arg903Lys
NP_001316055.1:p.Arg908Lys
NM_015268.4:c.2708G>A
More... 		05/25/2023 missense variant benign|likely benign DNAJC13-related condition; none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:DNAJC13
Accession:NM_015268
Location:EXON

Gene Symbol:DNAJC13
Accession:NM_001329126
Location:EXON

Gene Symbol:DNAJC13
Accession:XM_047447819
Location:EXON

Gene Symbol:DNAJC13
Accession:XM_047447820
Location:EXON

.


Database
Acc Id
Source(s)
ClinVar RCV003427387 CLINVAR
  RCV003929133 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DNAJC13 CLINVAR
OMIM 614334 CLINVAR