RGD:156220817 Rat Genome Database

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Variant: RGD:156220817 -  Homo sapiens

RGD ID: 156220817
ClinVar ID: CV2104777
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SNRNP200  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 2 96,952,626
GRCh38 2 96,286,888
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_014014.5:c.3640-11C>T
NG_016973.1:g.23672C>T
NC_000002.12:g.96286888G>A
NC_000002.11:g.96952626G>A
 12/21/2021 intron variant likely benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:SNRNP200
Accession:NM_014014
Location:INTRON

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV002932449 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SNRNP200 CLINVAR
OMIM 601664 CLINVAR