RGD:150487603 Rat Genome Database

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Variant: RGD:150487603 -  Homo sapiens

RGD ID: 150487603
RS ID: rs77726535
ClinVar ID: CV1225936
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PIEZO1  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 16 88,794,205
GRCh38 16 88,727,797
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1137t1:c.3197-136C>G
NM_001142864.4:c.3197-136C>G
LRG_1137:g.62424C>G
NG_042229.1:g.62424C>G
More... 		07/06/2018 intron variant benign none provided

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001618097 CLINVAR
dbSNP (RS) rs77726535 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PIEZO1 CLINVAR
OMIM 611184 CLINVAR