RGD:405131356 Rat Genome Database

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Variant: RGD:405131356 -  Homo sapiens

RGD ID: 405131356
ClinVar ID: CV2959068
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC16A12  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 10 91,192,931
GRCh38 10 89,433,174
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_213606.4:c.1441A>C
NG_021179.1:g.107383A>C
NC_000010.11:g.89433174T>G
NC_000010.10:g.91192931T>G
More... 		10/03/2023 missense variant uncertain significance none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003668406 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLC16A12 CLINVAR
OMIM 611910 CLINVAR