RGD:156184766 Rat Genome Database

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Variant: RGD:156184766 -  Homo sapiens

RGD ID: 156184766
ClinVar ID: CV2020626
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SNRNP200  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 2 96,966,722
GRCh38 2 96,300,984
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_014014.5:c.630+14A>C
NG_016973.1:g.9576A>C
NC_000002.12:g.96300984T>G
NC_000002.11:g.96966722T>G
 05/10/2022 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 RCV002710895 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SNRNP200 CLINVAR
OMIM 601664 CLINVAR