RGD:405137115 Rat Genome Database

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Variant: RGD:405137115 -  Homo sapiens

RGD ID: 405137115
ClinVar ID: CV2954380
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PIEZO1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 16 88,786,840
GRCh38 16 88,720,432
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1137:g.69789G>A
NG_042229.1:g.69789G>A
NC_000016.10:g.88720432C>T
NC_000016.9:g.88786840C>T
More... 		10/10/2023 missense variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003672909 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PIEZO1 CLINVAR
OMIM 611184 CLINVAR