RGD:155725126 Rat Genome Database

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Variant: RGD:155725126 -  Homo sapiens

RGD ID: 155725126
ClinVar ID: CV1824902
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC130004273  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 10 89,623,292
GRCh38 10 87,863,535
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
LRG_311t1:c.-934G>A
NM_001304718.1:c.-1639G>A
NM_001304717.4:c.-415G>A
NM_000314.6:c.-934G>A
More... 		08/30/2016 uncertain significance Cancer predisposition; Hereditary Cancer Syndrome; Hereditary neoplastic syndrome; Neoplastic Syndromes, Hereditary; Tumor predisposition
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV002450087 CLINVAR
MedGen C0027672 CLINVAR
NCBI Gene LOC130004273 CLINVAR
  PTEN CLINVAR
OMIM 601728 CLINVAR
SNOMED CT 699346009 CLINVAR