RGD:11088350 Rat Genome Database

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Variant: RGD:11088350 -  Homo sapiens

RGD ID: 11088350
RS ID: rs567739104
ClinVar ID: CV231760
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KLLN  LOC130004273  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 10 89,623,280
GRCh38 10 87,863,523
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_311:g.5086C>T
NG_007466.2:g.5086C>T
NC_000010.11:g.87863523C>T
NC_000010.10:g.89623280C>T
More... 		10/20/2021 5 prime utr variant uncertain significance 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 RCV000213464 CLINVAR
  RCV001358713 CLINVAR
dbSNP (RS) rs567739104 CLINVAR
MedGen C3661900 CLINVAR
  CN169374 CLINVAR
NCBI Gene KLLN CLINVAR
  LOC130004273 CLINVAR
  PTEN CLINVAR
OMIM 601728 CLINVAR
  612105 CLINVAR