RGD:405238802 Rat Genome Database

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Variant: RGD:405238802 -  Homo sapiens

RGD ID: 405238802
ClinVar ID: CV3081356
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PIEZO1  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 16 88,782,057
GRCh38 16 88,715,649
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1137t1:c.7522C>A
NM_014745.1:c.6064C>A
NM_001142864.4:c.7522C>A
LRG_1137:g.74572C>A
More... 		03/29/2023 missense variant uncertain significance none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV003736441 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PIEZO1 CLINVAR
OMIM 611184 CLINVAR