RGD:150443691 Rat Genome Database

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Variant: RGD:150443691 -  Homo sapiens

RGD ID: 150443691
RS ID: rs546957695
ClinVar ID: CV1264630
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NEK8  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 17 27,061,631
GRCh38 17 28,734,613
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.254-159G>A
NG_012263.1:g.10800G>A
NC_000017.11:g.28734613G>A
NC_000017.10:g.27061631G>A
 09/19/2019 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:NEK8
Accession:NM_178170
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001679614 CLINVAR
dbSNP (RS) rs546957695 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NEK8 CLINVAR
OMIM 609799 CLINVAR