RGD:405251506 Rat Genome Database

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Variant: RGD:405251506 -  Homo sapiens

RGD ID: 405251506
ClinVar ID: CV3181346
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KLHL9  LOC107987053  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 9 21,333,157
GRCh38 9 21,333,158
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_018847.4:c.1702G>A
NG_051240.1:g.7275G>A
NC_000009.12:g.21333158C>T
NC_000009.11:g.21333157C>T
More... 		05/15/2023 missense variant uncertain significance none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003870348 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene KLHL9 CLINVAR
OMIM 611201 CLINVAR