RGD:13509821 Rat Genome Database

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Variant: RGD:13509821 -  Homo sapiens

RGD ID: 13509821
RS ID: rs1028802765
ClinVar ID: CV481913
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KLLN  LOC130004273  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 10 89,623,151
GRCh38 10 87,863,394
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000010.11:g.87863394A>C
LRG_311:g.4957A>C
NG_007466.2:g.4957A>C
LRG_311t1:c.-1075A>C
More... 		08/09/2016 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 RCV000578975 CLINVAR
dbSNP (RS) rs1028802765 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene KLLN CLINVAR
  LOC130004273 CLINVAR
  PTEN CLINVAR
OMIM 601728 CLINVAR
  612105 CLINVAR