RGD:407497418 Rat Genome Database

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Variant: RGD:407497418 -  Homo sapiens

RGD ID: 407497418
ClinVar ID: CV3437533
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DNAJC13  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 3 132,198,123
GRCh38 3 132,479,279
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NG_051045.1:g.66753T>C
NC_000003.12:g.132479279T>C
NC_000003.11:g.132198123T>C
NM_015268.3:c.2762T>C
More... 		04/09/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004622195 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene DNAJC13 CLINVAR
OMIM 614334 CLINVAR