RGD:11659402 Rat Genome Database

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Variant: RGD:11659402 -  Homo sapiens

RGD ID: 11659402
RS ID: rs886052772
ClinVar ID: CV327921
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NEK8  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 17 27,069,768
GRCh38 17 28,742,750
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_012263.1:g.18937A>G
NC_000017.11:g.28742750A>G
NC_000017.10:g.27069768A>G
NM_178170.3:c.*763A>G
More... 		06/14/2016 3 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:NEK8
Accession:NM_178170
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000357635 CLINVAR
dbSNP (RS) rs886052772 CLINVAR
MedGen C3151188 CLINVAR
NCBI Gene NEK8 CLINVAR
OMIM 609799 CLINVAR
  613824 CLINVAR