RGD:150489202 Rat Genome Database

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Variant: RGD:150489202 -  Homo sapiens

RGD ID: 150489202
RS ID: rs115505660
ClinVar ID: CV1208389
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NEK8  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 17 27,068,312
GRCh38 17 28,741,294
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.1891+58G>C
NG_012263.1:g.17481G>C
NC_000017.11:g.28741294G>C
NC_000017.10:g.27068312G>C
 04/28/2020 intron variant likely 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 RCV001592249 CLINVAR
dbSNP (RS) rs115505660 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NEK8 CLINVAR
OMIM 609799 CLINVAR