RGD:151351167 Rat Genome Database

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Variant: RGD:151351167 -  Homo sapiens

RGD ID: 151351167
RS ID: rs1264379107
ClinVar ID: CV1321082
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127885143  PIEZO1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 16 88,851,390
GRCh38 16 88,784,982
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_042229.1:g.5239G>A
LRG_1137t1:c.-18G>A
LRG_1137:g.5239G>A
NC_000016.10:g.88784982C>T
More... 		11/02/2020 5 prime utr variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PIEZO1
Accession:NM_001142864
Location:5UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001810766 CLINVAR
dbSNP (RS) rs1264379107 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PIEZO1 CLINVAR
OMIM 611184 CLINVAR