RGD:597643882 Rat Genome Database

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Variant: RGD:597643882 -  Homo sapiens

RGD ID: 597643882
ClinVar ID: CV3662945
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DNAJC13  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 3 132,166,199
GRCh38 3 132,447,355
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001329126.2:c.179T>C
NM_015268.4:c.179T>C
NG_051045.1:g.34829T>C
NC_000003.12:g.132447355T>C
More... 		11/10/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004909558 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene DNAJC13 CLINVAR
OMIM 614334 CLINVAR