RGD:10042828 Rat Genome Database

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Variant: RGD:10042828 -  Homo sapiens

RGD ID: 10042828
RS ID: rs1554889805
ClinVar ID: CV187278
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KLLN  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 10 89,622,992
GRCh38 10 87,863,235
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_311:g.4798C>G
NG_007466.2:g.4798C>G
NC_000010.11:g.87863235C>G
NC_000010.10:g.89622992C>G
More... 		01/27/2014 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 RCV000115560 CLINVAR
dbSNP (RS) rs1554889805 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene KLLN CLINVAR
  PTEN CLINVAR
OMIM 601728 CLINVAR
  612105 CLINVAR