RGD:150411714 Rat Genome Database

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Variant: RGD:150411714 -  Homo sapiens

RGD ID: 150411714
RS ID: rs74597321
ClinVar ID: CV1191863
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PIEZO1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 16 88,792,529
GRCh38 16 88,726,121
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1137t1:c.3968+163C>T
NM_001142864.4:c.3968+163C>T
NG_042229.1:g.64100C>T
LRG_1137:g.64100C>T
More... 		07/09/2018 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 RCV001566686 CLINVAR
dbSNP (RS) rs74597321 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PIEZO1 CLINVAR
OMIM 611184 CLINVAR