RGD:15160487 Rat Genome Database

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Variant: RGD:15160487 -  Homo sapiens

RGD ID: 15160487
RS ID: rs148264536
ClinVar ID: CV744968
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ARL2BP  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 16 57,286,068
GRCh38 16 57,252,156
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.391-10T>A
NG_033905.1:g.12031T>A
NC_000016.10:g.57252156T>A
NC_000016.9:g.57286068T>A
More... 		12/14/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ARL2BP
Accession:NM_012106
Location:INTRON

Gene Symbol:ARL2BP
Accession:XM_047433883
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000903156 CLINVAR
dbSNP (RS) rs148264536 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ARL2BP CLINVAR
OMIM 615407 CLINVAR