RGD:404993903 Rat Genome Database

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Variant: RGD:404993903 -  Homo sapiens

RGD ID: 404993903
ClinVar ID: CV3132384
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SNRNP200  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 2 96,964,013
GRCh38 2 96,298,275
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_014014.5:c.1119+9T>C
NG_016973.1:g.12285T>C
NC_000002.12:g.96298275A>G
NC_000002.11:g.96964013A>G
 05/21/2023 intron variant uncertain significance none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:SNRNP200
Accession:NM_014014
Location:INTRON

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV003827322 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SNRNP200 CLINVAR
OMIM 601664 CLINVAR