RGD:15126646 Rat Genome Database

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Variant: RGD:15126646 -  Homo sapiens

RGD ID: 15126646
RS ID: rs370692905
ClinVar ID: CV760901
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NONO  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 X 70,518,676
GRCh38 X 71,298,826
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.1014+10C>T
NM_001145408.2:c.1281+10C>T
NM_001145409.2:c.1281+10C>T
NM_007363.5:c.1281+10C>T
More... 		01/26/2018 intron variant likely benign none provided

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

Gene Symbol:NONO
Accession:NM_001145409
Location:INTRON

Gene Symbol:NONO
Accession:NM_001145408
Location:INTRON

Gene Symbol:NONO
Accession:NM_007363
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000919362 CLINVAR
dbSNP (RS) rs370692905 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NONO CLINVAR
OMIM 300084 CLINVAR