RGD:405249074 Rat Genome Database

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Variant: RGD:405249074 -  Homo sapiens

RGD ID: 405249074
ClinVar ID: CV3003920
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ARL2BP  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 16 57,279,337
GRCh38 16 57,245,425
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_012106.4:c.38+20C>T
NG_033905.1:g.5300C>T
NG_193509.1:g.548C>T
NG_193510.1:g.78C>T
More... 		03/01/2023 intron variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003721263 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ARL2BP CLINVAR
OMIM 615407 CLINVAR