RGD:25323644 Rat Genome Database

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Variant: RGD:25323644 -  Homo sapiens

RGD ID: 25323644
RS ID: rs1589593482
ClinVar ID: CV815431
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KLLN  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 10 89,622,942
GRCh38 10 87,863,185
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_311t1:c.-1284C>T
LRG_311:g.4748C>T
NG_007466.2:g.4748C>T
NG_033079.1:g.5253G>A
More... 		06/07/2018 5 prime utr variant 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 Transcripts
Gene Symbol:KLLN
Accession:NM_001126049
Location:5UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001010748 CLINVAR
dbSNP (RS) rs1589593482 CLINVAR
MedGen C0027672 CLINVAR
NCBI Gene KLLN CLINVAR
  PTEN CLINVAR
OMIM 601728 CLINVAR
  612105 CLINVAR
SNOMED CT 699346009 CLINVAR