RGD:408370421 Rat Genome Database

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Variant: RGD:408370421 -  Homo sapiens

RGD ID: 408370421
ClinVar ID: CV3510146
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DNAJC13  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 3 132,172,152
GRCh38 3 132,453,308
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001329126.2:c.548C>T
NM_015268.4:c.548C>T
NG_051045.1:g.40782C>T
NC_000003.12:g.132453308C>T
More... 		08/09/2024 missense variant uncertain significance DNAJC13-related condition

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Database
Acc Id
Source(s)
ClinVar RCV004739769 CLINVAR
NCBI Gene DNAJC13 CLINVAR
OMIM 614334 CLINVAR