RGD:13520553 Rat Genome Database

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Variant: RGD:13520553 -  Homo sapiens

RGD ID: 13520553
RS ID: rs786203419
ClinVar ID: CV495487
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC130004273  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 10 89,623,293
GRCh38 10 87,863,536
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
LRG_311:g.5099G>C
NG_007466.2:g.5099G>C
NC_000010.11:g.87863536G>C
NC_000010.10:g.89623293G>C
More... 		11/06/2019 uncertain significance 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 Information

Database Acc Id Source(s)
ClinVar RCV000598726 CLINVAR
  RCV002377240 CLINVAR
dbSNP (RS) rs786203419 CLINVAR
MedGen C0027672 CLINVAR
  C3661900 CLINVAR
NCBI Gene LOC130004273 CLINVAR
  PTEN CLINVAR
OMIM 601728 CLINVAR
SNOMED CT 699346009 CLINVAR