RGD:156312989 Rat Genome Database

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Variant: RGD:156312989 -  Homo sapiens

RGD ID: 156312989
ClinVar ID: CV1913746
Genic Status: GENIC
Type: deletion (SO:0000159) 
Associated Genes: NDUFAF5  
Reference Nucleotide: G
Variant Nucleotide: -
Position
Assembly Chr Position
GRCh37 20 13,797,109
GRCh38 20 13,816,463
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Clinical Significance
Trait Synonyms
NG_015811.2:g.36437del
NC_000020.11:g.13816463del
NC_000020.10:g.13797108del
NC_000020.10:g.13797109del
More... 		09/28/2023 pathogenic none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

.
PMID:28492532   PMID:29581464   PMID:30581749   PMID:34177781  



Database
Acc Id
Source(s)
ClinVar RCV002599768 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NDUFAF5 CLINVAR
OMIM 612360 CLINVAR