RGD:150446764 Rat Genome Database

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Variant: RGD:150446764 -  Homo sapiens

RGD ID: 150446764
RS ID: rs11643304
ClinVar ID: CV1215705
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HSALR1  LOC130059751  PIEZO1  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 16 88,803,934
GRCh38 16 88,737,526
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1137t1:c.1195+33T>G
NM_001142864.4:c.1195+33T>G
LRG_1137:g.52695T>G
NG_042229.1:g.52695T>G
More... 		07/09/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PIEZO1
Accession:NM_001142864
Location:INTRON

Gene Symbol:HSALR1
Accession:NR_103774
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001611298 CLINVAR
dbSNP (RS) rs11643304 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LOC100289580 CLINVAR
  LOC130059751 CLINVAR
  PIEZO1 CLINVAR
OMIM 611184 CLINVAR