RGD:407497404 Rat Genome Database

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Variant: RGD:407497404 -  Homo sapiens

RGD ID: 407497404
ClinVar ID: CV3437529
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DNAJC13  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 3 132,202,364
GRCh38 3 132,483,520
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_015268.4:c.3125A>G
NM_001329126.2:c.3140A>G
NG_051045.1:g.70994A>G
NC_000003.12:g.132483520A>G
More... 		04/04/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004622191 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene DNAJC13 CLINVAR
OMIM 614334 CLINVAR