RGD:15143631 Rat Genome Database

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Variant: RGD:15143631 -  Homo sapiens

RGD ID: 15143631
RS ID: rs746490648
ClinVar ID: CV787266
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HSPA9  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 5 137,893,684
GRCh38 5 138,557,995
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_004134.7:c.1516-9T>G
NG_029469.1:g.22635T>G
NC_000005.10:g.138557995A>C
NC_000005.9:g.137893684A>C
More... 		01/14/2019 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:HSPA9
Accession:NM_004134
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000983359 CLINVAR
dbSNP (RS) rs746490648 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene HSPA9 CLINVAR
OMIM 600548 CLINVAR