RGD:12901477 Rat Genome Database

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Variant: RGD:12901477 -  Homo sapiens

RGD ID: 12901477
RS ID: rs1064795081
ClinVar ID: CV407962
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KLLN  LOC130004273  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 10 89,623,281
GRCh38 10 87,863,524
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_311:g.5087G>A
NG_007466.2:g.5087G>A
NC_000010.11:g.87863524G>A
NC_000010.10:g.89623281G>A
More... 		06/01/2016 5 prime utr variant uncertain significance|no classifications from unflagged records AllHighlyPenetrant; none provided

Variant Details
Variant Transcripts
Gene Symbol:KLLN
Accession:NM_001126049
Location:5UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000484771 CLINVAR
  RCV001507279 CLINVAR
dbSNP (RS) rs1064795081 CLINVAR
MedGen C3661900 CLINVAR
  CN169374 CLINVAR
NCBI Gene KLLN CLINVAR
  LOC130004273 CLINVAR
  PTEN CLINVAR
OMIM 601728 CLINVAR
  612105 CLINVAR