RGD:150477445 Rat Genome Database

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Variant: RGD:150477445 -  Homo sapiens

RGD ID: 150477445
RS ID: rs11640422
ClinVar ID: CV1218627
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PIEZO1  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 16 88,809,105
GRCh38 16 88,742,697
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1137t1:c.161-275T>A
NM_001142864.4:c.161-275T>A
LRG_1137:g.47524T>A
NG_042229.1:g.47524T>A
More... 		07/09/2018 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 RCV001616254 CLINVAR
dbSNP (RS) rs11640422 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PIEZO1 CLINVAR
OMIM 611184 CLINVAR