RGD:405140642 Rat Genome Database

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Variant: RGD:405140642 -  Homo sapiens

RGD ID: 405140642
ClinVar ID: CV3026215
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC12A3  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 16 56,916,321
GRCh38 16 56,882,409
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001126107.2:c.1578C>T
NM_001410896.1:c.1578C>T
NM_000339.3:c.1581C>T
NM_001126108.2:c.1581C>T
More... 		09/08/2023 synonymous variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003702477 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLC12A3 CLINVAR
OMIM 600968 CLINVAR