RGD:28896544 Rat Genome Database

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Variant: RGD:28896544 -  Homo sapiens

RGD ID: 28896544
RS ID: rs1228540616
ClinVar ID: CV877116
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NEK8  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 17 27,069,764
GRCh38 17 28,742,746
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_178170.3:c.*759C>G
NG_012263.1:g.18933C>G
NC_000017.11:g.28742746C>G
NC_000017.10:g.27069764C>G
More... 		01/13/2018 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 RCV001122883 CLINVAR
dbSNP (RS) rs1228540616 CLINVAR
MedGen C3151188 CLINVAR
NCBI Gene NEK8 CLINVAR
OMIM 609799 CLINVAR
  613824 CLINVAR