RGD:405208681 Rat Genome Database

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Variant: RGD:405208681 -  Homo sapiens

RGD ID: 405208681
ClinVar ID: CV3145737
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PIEZO1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 16 88,793,103
GRCh38 16 88,726,695
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1137t1:c.3699+20G>A
NM_001142864.4:c.3699+20G>A
LRG_1137:g.63526G>A
NG_042229.1:g.63526G>A
More... 		08/14/2023 intron variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003845467 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PIEZO1 CLINVAR
OMIM 611184 CLINVAR