RGD:151352385 Rat Genome Database

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Variant: RGD:151352385 -  Homo sapiens

RGD ID: 151352385
RS ID: rs756049905
ClinVar ID: CV1321340
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PIEZO1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 16 88,786,465
GRCh38 16 88,720,057
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1137t1:c.6164+12C>T
NM_001142864.4:c.6164+12C>T
LRG_1137:g.70164C>T
NG_042229.1:g.70164C>T
More... 		10/20/2020 intron variant likely 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 RCV001811788 CLINVAR
dbSNP (RS) rs756049905 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PIEZO1 CLINVAR
OMIM 611184 CLINVAR