RGD:15154713 Rat Genome Database

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Variant: RGD:15154713 -  Homo sapiens

RGD ID: 15154713
RS ID: rs185385178
ClinVar ID: CV749213
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HSPA4  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 5 132,409,020
GRCh38 5 133,073,328
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_002154.4:c.528A>G
NC_000005.10:g.133073328A>G
NC_000005.9:g.132409020A>G
NM_002154.3:c.528A>G
More...
05/18/2018 synonymous variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:HSPA4
Accession:NM_002154
Location:EXON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000924315 CLINVAR
dbSNP (RS) rs185385178 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene HSPA4 CLINVAR
OMIM 601113 CLINVAR