rs886057506 Rat Genome Database

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Variant: rs886057506 -  Homo sapiens

RGD ID: 11660446
RS ID: rs886057506
ClinVar ID: CV347776
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127896356  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 22 41,253,099
GRCh38 22 40,857,095
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NG_028221.1:g.5015C>T
NC_000022.11:g.40857095C>T
NC_000022.10:g.41253099C>T
NM_001204827.1:c.-87C>T
More... 		06/14/2016 5 prime utr variant uncertain significance
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
CV347776Humannephronophthisis-like nephropathy 1  IAGP 8554872ClinVar Annotator: match by term: Nephronophthisis-like nephropathy 1ClinVarPMID:25741868


.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV000367240 CLINVAR
  RCV005027444 CLINVAR
dbSNP (RS) rs886057506 CLINVAR
MedGen C3150419 CLINVAR
  C3280617 CLINVAR
NCBI Gene XPNPEP3 CLINVAR
OMIM 613159 CLINVAR
  613553 CLINVAR