RGD:150443275 Rat Genome Database

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Variant: RGD:150443275 -  Homo sapiens

RGD ID: 150443275
RS ID: rs11076707
ClinVar ID: CV1249258
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PIEZO1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 16 88,808,111
GRCh38 16 88,741,703
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1137t1:c.327-87A>G
NM_001142864.4:c.327-87A>G
LRG_1137:g.48518A>G
NG_042229.1:g.48518A>G
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 RCV001666690 CLINVAR
dbSNP (RS) rs11076707 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PIEZO1 CLINVAR
OMIM 611184 CLINVAR