RGD:401854303 Rat Genome Database

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Variant: RGD:401854303 -  Homo sapiens

RGD ID: 401854303
ClinVar ID: CV2749281
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KLLN  LOC130004273  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 10 89,623,284
GRCh38 10 87,863,527
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_007466.2:g.5090G>T
NC_000010.11:g.87863527G>T
NC_000010.10:g.89623284G>T
LRG_1087:g.4911C>A
More... 		08/15/2023 5 prime utr variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:KLLN
Accession:NM_001126049
Location:5UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV003330479 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene KLLN CLINVAR
  LOC130004273 CLINVAR
  PTEN CLINVAR
OMIM 601728 CLINVAR
  612105 CLINVAR