RGD:25315697 Rat Genome Database

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Variant: RGD:25315697 -  Homo sapiens

RGD ID: 25315697
RS ID: rs786203535
ClinVar ID: CV810056
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KLLN  LOC130004273  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 10 89,623,247
GRCh38 10 87,863,490
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.5053C>A
NC_000010.11:g.87863490C>A
NM_001126049.2:c.-1003G>T
LRG_1087t1:c.-1003G>T
More... 		01/17/2019 5 prime utr variant uncertain significance Cancer predisposition; Hereditary Cancer Syndrome; Hereditary neoplastic syndrome; Neoplastic Syndromes, Hereditary; Tumor predisposition
Disease Annotations     Click to see Annotation Detail View


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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001019762 CLINVAR
dbSNP (RS) rs786203535 CLINVAR
MedGen C0027672 CLINVAR
NCBI Gene KLLN CLINVAR
  LOC130004273 CLINVAR
  PTEN CLINVAR
OMIM 601728 CLINVAR
  612105 CLINVAR
SNOMED CT 699346009 CLINVAR