RGD:405132857 Rat Genome Database

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Variant: RGD:405132857 -  Homo sapiens

RGD ID: 405132857
ClinVar ID: CV3115207
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TRPM6  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 9 77,457,178
GRCh38 9 74,842,262
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001177310.2:c.219T>C
NM_001177311.2:c.219T>C
NM_017662.5:c.234T>C
NG_017036.1:g.50833T>C
More... 		11/04/2023 synonymous variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003816052 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TRPM6 CLINVAR
OMIM 607009 CLINVAR