RGD:405139516 Rat Genome Database

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Variant: RGD:405139516 -  Homo sapiens

RGD ID: 405139516
ClinVar ID: CV3029496
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PIEZO1  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 16 88,782,145
GRCh38 16 88,715,737
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1137t1:c.7434C>G
NM_014745.1:c.5976C>G
NM_001142864.4:c.7434C>G
LRG_1137:g.74484C>G
More... 		12/11/2023 synonymous variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003702282 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PIEZO1 CLINVAR
OMIM 611184 CLINVAR