RGD:10042833 Rat Genome Database

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Variant: RGD:10042833 -  Homo sapiens

RGD ID: 10042833
RS ID: rs786205433
ClinVar ID: CV187290
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KLLN  LOC130004273  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 10 89,623,270
GRCh38 10 87,863,513
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_311:g.5076G>C
NG_007466.2:g.5076G>C
NC_000010.11:g.87863513G>C
NC_000010.10:g.89623270G>C
More... 		12/16/2019 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 RCV000115578 CLINVAR
dbSNP (RS) rs786205433 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene KLLN CLINVAR
  LOC130004273 CLINVAR
  PTEN CLINVAR
OMIM 601728 CLINVAR
  612105 CLINVAR