rs769353145 Rat Genome Database

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Variant: rs769353145 -  Homo sapiens

RGD ID: 152125757
RS ID: rs769353145
ClinVar ID: CV1665837
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ARL2BP  LOC124903697  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 16 57,283,717
GRCh38 16 57,249,805
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_012106.4:c.246G>A
NG_033905.1:g.9680G>A
NC_000016.10:g.57249805G>A
NC_000016.9:g.57283717G>A
More... 		02/10/2023 synonymous variant likely benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:ARL2BP
Accession:NM_012106
Location:EXON
Amino Acid Prediction: L to L (synonymous)
Amino Acid Position: 82
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MDALEGESFALSFSSASDAEFDAVVGYLEDIIMDDEFQLLQRNFMDKYYLEFEDTEENKLIYTPIFNEYISLVEKYIEEQ
LLQRIPEFNMAAFTTTLQHHKDEVAGDIFDMLLTFTDFLAFKEMFLDYRAEKEGRGLDLSSGLVVTSLCKSSSLPASQNN
LRH*

Gene Symbol:ARL2BP
Accession:XM_047433883
Location:EXON
Amino Acid Prediction: L to L (synonymous)
Amino Acid Position: 50
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MDDEFQLLQRNFMDKYYLEFEDTEENKLIYTPIFNEYISLVEKYIEEQLLQRIPEFNMAAFTTTLQHHKDEVAGDIFDML
LTFTDFLAFKEMFLDYRAEKEGRGLDLSSGLVVTSLCKSSSLPASQNNLRH*

Gene Symbol:LOC124903697
Accession:XR_007065082
Location:EXON;NON-CODING

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV002198650 CLINVAR
dbSNP (RS) rs769353145 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ARL2BP CLINVAR
OMIM 615407 CLINVAR