RGD:597754895 Rat Genome Database

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Variant: RGD:597754895 -  Homo sapiens

RGD ID: 597754895
ClinVar ID: CV3606340
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC25A32  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 8 104,417,034
GRCh38 8 103,404,806
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_030780.5:c.361A>G
NG_047200.1:g.15530A>G
NC_000008.11:g.103404806T>C
NC_000008.10:g.104417034T>C
More... 		10/12/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004867973 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene SLC25A32 CLINVAR
OMIM 138480 CLINVAR