RGD:152032805 Rat Genome Database

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Variant: RGD:152032805 -  Homo sapiens

RGD ID: 152032805
RS ID: rs2113100160
ClinVar ID: CV1643185
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SPARC  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 5 151,052,797
GRCh38 5 151,673,236
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_003118.4:c.121-20T>C
NG_042174.1:g.18819T>C
NC_000005.10:g.151673236A>G
NC_000005.9:g.151052797A>G
More... 		06/06/2021 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SPARC
Accession:NM_003118
Location:INTRON

Gene Symbol:SPARC
Accession:NM_001309444
Location:INTRON

Gene Symbol:SPARC
Accession:NM_001309443
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002205050 CLINVAR
dbSNP (RS) rs2113100160 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SPARC CLINVAR
OMIM 182120 CLINVAR