RGD:13509813 Rat Genome Database

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Variant: RGD:13509813 -  Homo sapiens

RGD ID: 13509813
RS ID: rs1554889924
ClinVar ID: CV481931
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC130004273  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 10 89,623,297
GRCh38 10 87,863,540
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
LRG_311t1:c.-929G>A
NC_000010.11:g.87863540G>A
NC_000010.10:g.89623297G>A
LRG_311:g.5103G>A
More... 		03/30/2023 uncertain significance AllHighlyPenetrant; Cancer predisposition; Hereditary Cancer Syndrome; Hereditary neoplastic syndrome; Neoplastic Syndromes, Hereditary; none provided; Tumor predisposition
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples
Additional References at PubMed
PMID:12844284   PMID:21417916   PMID:23315997  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000578958 CLINVAR
  RCV001194182 CLINVAR
  RCV002377199 CLINVAR
dbSNP (RS) rs1554889924 CLINVAR
MedGen C0027672 CLINVAR
  C3661900 CLINVAR
  CN169374 CLINVAR
NCBI Gene LOC130004273 CLINVAR
  PTEN CLINVAR
OMIM 601728 CLINVAR
SNOMED CT 699346009 CLINVAR