rs10024487 Rat Genome Database

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Variant: rs10024487 -  Homo sapiens

RGD ID: 150404799
RS ID: rs10024487
ClinVar ID: CV1178896
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ADAMTS3  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 4 73,175,093
GRCh38 4 72,309,376
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000004.11:g.73175093C>T
NM_014243.3:c.2179+21G>A
NC_000004.12:g.72309376C>T
NG_046955.1:g.264424G>A
 07/14/2021 intron variant benign none provided
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:ADAMTS3
Accession:NM_014243
Location:INTRON

Gene Symbol:ADAMTS3
Accession:XM_011532421
Location:INTRON

Gene Symbol:ADAMTS3
Accession:XM_011532422
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001549242 CLINVAR
  RCV004716773 CLINVAR
dbSNP (RS) rs10024487 CLINVAR
MedGen C3661900 CLINVAR
  C4748408 CLINVAR
NCBI Gene ADAMTS3 CLINVAR
OMIM 605011 CLINVAR
  618154 CLINVAR