RGD:156061603 Rat Genome Database

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Variant: RGD:156061603 -  Homo sapiens

RGD ID: 156061603
ClinVar ID: CV2044874
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PIEZO1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 16 88,789,421
GRCh38 16 88,723,013
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1137t1:c.4496-4G>A
NM_001142864.4:c.4496-4G>A
LRG_1137:g.67208G>A
NG_042229.1:g.67208G>A
More... 		12/25/2021 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PIEZO1
Accession:NM_001142864
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002736857 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PIEZO1 CLINVAR
OMIM 611184 CLINVAR