RGD:10042361 Rat Genome Database

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Variant: RGD:10042361 -  Homo sapiens

RGD ID: 10042361
RS ID: rs786204913
ClinVar ID: CV187275
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KLLN  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 10 89,622,885
GRCh38 10 87,863,128
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_311:g.4691G>A
NG_007466.2:g.4691G>A
NC_000010.11:g.87863128G>A
NC_000010.10:g.89622885G>A
More... 		07/09/2014 2kb upstream variant|5 prime utr variant uncertain significance 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 RCV000169854 CLINVAR
dbSNP (RS) rs786204913 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene KLLN CLINVAR
  PTEN CLINVAR
OMIM 601728 CLINVAR
  612105 CLINVAR