RGD:597749479 Rat Genome Database

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Variant: RGD:597749479 -  Homo sapiens

RGD ID: 597749479
ClinVar ID: CV3612450
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TARS3  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 15 102,241,337
GRCh38 15 101,701,134
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_152334.3:c.1272C>G
NC_000015.10:g.101701134G>C
NC_000015.9:g.102241337G>C
NM_152334.2:c.1272C>G
More... 		11/07/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004866467 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene TARS3 CLINVAR