RGD:597700074 Rat Genome Database

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Variant: RGD:597700074 -  Homo sapiens

RGD ID: 597700074
ClinVar ID: CV3606249
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127885554  SLC25A11  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 17 4,841,169
GRCh38 17 4,937,874
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001165418.2:c.659G>A
NM_001165417.2:c.779G>A
NM_003562.5:c.812G>A
NG_135295.1:g.173C>T
More... 		11/19/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004859822 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene SLC25A11 CLINVAR
OMIM 604165 CLINVAR