RGD:405204949 Rat Genome Database

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Variant: RGD:405204949 -  Homo sapiens

RGD ID: 405204949
ClinVar ID: CV3144171
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NONO  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 70,517,727
GRCh38 X 71,297,877
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001145408.2:c.1070G>A
NM_001145409.2:c.1070G>A
NM_007363.5:c.1070G>A
NM_001145410.2:c.803G>A
More... 		09/05/2023 missense variant uncertain significance none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003844961 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NONO CLINVAR
OMIM 300084 CLINVAR