RGD:405164505 Rat Genome Database

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Variant: RGD:405164505 -  Homo sapiens

RGD ID: 405164505
ClinVar ID: CV2905689
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NONO  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 X 70,514,266
GRCh38 X 71,294,416
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001145410.2:c.271A>G
NM_001145408.2:c.538A>G
NM_001145409.2:c.538A>G
NM_007363.5:c.538A>G
More... 		07/08/2023 missense variant uncertain significance none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003562630 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NONO CLINVAR
OMIM 300084 CLINVAR