RGD:597683836 Rat Genome Database

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Variant: RGD:597683836 -  Homo sapiens

RGD ID: 597683836
ClinVar ID: CV3673834
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DTWD1  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 15 49,935,533
GRCh38 15 49,643,336
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_020234.5:c.673T>A
NP_001138427.1:p.Leu225Ile
NP_064619.2:p.Leu225Ile
NM_001144955.2:c.673T>A
More... 		09/25/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004914536 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene DTWD1 CLINVAR