RGD:13509734 Rat Genome Database

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Variant: RGD:13509734 -  Homo sapiens

RGD ID: 13509734
RS ID: rs889785939
ClinVar ID: CV481930
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC130004273  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 10 89,623,294
GRCh38 10 87,863,537
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NG_033079.1:g.4901C>T
LRG_311t1:c.-932G>A
NG_007466.2:g.5100G>A
LRG_311:g.5100G>A
More... 		12/29/2020 uncertain significance AllHighlyPenetrant; none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000578716 CLINVAR
  RCV001821692 CLINVAR
dbSNP (RS) rs889785939 CLINVAR
MedGen C3661900 CLINVAR
  CN169374 CLINVAR
NCBI Gene LOC130004273 CLINVAR
  PTEN CLINVAR
OMIM 601728 CLINVAR