RGD:13509751 Rat Genome Database

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Variant: RGD:13509751 -  Homo sapiens

RGD ID: 13509751
RS ID: rs1554889925
ClinVar ID: CV481933
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC130004273  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 10 89,623,301
GRCh38 10 87,863,544
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NC_000010.10:g.89623301G>A
NG_007466.2:g.5107G>A
NC_000010.11:g.87863544G>A
LRG_311t1:c.-925G>A
More... 		02/08/2017 uncertain significance none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000578833 CLINVAR
dbSNP (RS) rs1554889925 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LOC130004273 CLINVAR
  PTEN CLINVAR
OMIM 601728 CLINVAR