RGD:405112463 Rat Genome Database

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Variant: RGD:405112463 -  Homo sapiens

RGD ID: 405112463
ClinVar ID: CV3133607
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CRAT  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 131,858,367
GRCh38 9 129,096,088
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000009.11:g.131858367C>A
NR_028048.1:n.1956G>T
NP_001333478.2:p.Leu485=
NP_001244292.2:p.Leu504=
More... 		05/12/2023 synonymous variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003836400 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CRAT CLINVAR
OMIM 600184 CLINVAR