RGD:150481657 Rat Genome Database

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Variant: RGD:150481657 -  Homo sapiens

RGD ID: 150481657
RS ID: rs2340985
ClinVar ID: CV1222201
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HSALR1  PIEZO1  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 16 88,799,302
GRCh38 16 88,732,894
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1137:g.57327C>G
NG_042229.1:g.57327C>G
NC_000016.10:g.88732894G>C
NC_000016.9:g.88799302G>C
More... 		07/10/2018 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 RCV001616999 CLINVAR
dbSNP (RS) rs2340985 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LOC100289580 CLINVAR
  PIEZO1 CLINVAR
OMIM 611184 CLINVAR