RGD:15198887 Rat Genome Database

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Variant: RGD:15198887 -  Homo sapiens

RGD ID: 15198887
RS ID: rs778531510
ClinVar ID: CV759095
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HSPD1  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 2 198,363,392
GRCh38 2 197,498,668
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_002156.5:c.174+7G>C
NG_008914.1:g.3672C>G
NG_008915.1:g.6607G>C
NC_000002.12:g.197498668C>G
More... 		03/29/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:HSPD1
Accession:NM_002156
Location:INTRON

Gene Symbol:HSPD1
Accession:NM_199440
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000912384 CLINVAR
dbSNP (RS) rs778531510 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene HSPD1 CLINVAR
OMIM 118190 CLINVAR