RGD:150442111 Rat Genome Database

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Variant: RGD:150442111 -  Homo sapiens

RGD ID: 150442111
RS ID: rs112470710
ClinVar ID: CV1246839
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NONO  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 X 70,514,565
GRCh38 X 71,294,715
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_007363.5:c.650+187G>C
NG_046742.1:g.16524G>C
NC_000023.11:g.71294715G>C
NC_000023.10:g.70514565G>C
More... 		05/13/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:NONO
Accession:NM_001145410
Location:INTRON

Gene Symbol:NONO
Accession:NM_001145408
Location:INTRON

Gene Symbol:NONO
Accession:NM_007363
Location:INTRON

Gene Symbol:NONO
Accession:NM_001145409
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001666493 CLINVAR
dbSNP (RS) rs112470710 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NONO CLINVAR
OMIM 300084 CLINVAR