rs201141721 Rat Genome Database

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Variant: rs201141721 -  Homo sapiens

RGD ID: 28902528
RS ID: rs201141721
ClinVar ID: CV886684
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MRAP  URB1  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 21 33,684,321
GRCh38 21 32,312,010
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001285394.2:c.*14T>A
NM_178817.4:c.*14T>A
NM_014825.3:c.*2908A>T
NG_016234.1:g.25198T>A
More... 		01/13/2018 3 prime utr variant uncertain significance FAMILIAL GLUCOCORTICOID DEFICIENCY 2
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
CV886684HumanGlucocorticoid Deficiency 2  IAGP 8554872ClinVar Annotator: match by term: Glucocorticoid deficiency 2ClinVar 
Gene Symbol:URB1
Accession:NM_014825
Location:3UTRS;EXON

Gene Symbol:MRAP
Accession:NM_178817
Location:3UTRS;EXON

Gene Symbol:MRAP
Accession:NM_001285394
Location:3UTRS;EXON

Gene Symbol:MRAP
Accession:NM_001379228
Location:3UTRS;EXON

Gene Symbol:MRAP
Accession:NM_206898
Location:INTRON

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Database
Acc Id
Source(s)
ClinVar RCV001143612 CLINVAR
dbSNP (RS) rs201141721 CLINVAR
MedGen C4049714 CLINVAR
NCBI Gene MRAP CLINVAR
  URB1 CLINVAR
OMIM 607398 CLINVAR
  608865 CLINVAR
  609196 CLINVAR