RGD:151232560 Rat Genome Database

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Variant: RGD:151232560 -  Homo sapiens

RGD ID: 151232560
RS ID: rs2148039353
ClinVar ID: CV1316838
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NONO  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 70,517,311
GRCh38 X 71,297,461
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.1028G>A
NM_001145409.2:c.1028G>A
NM_007363.5:c.1028G>A
NM_001145410.2:c.761G>A
More... 		05/24/2021 missense variant uncertain significance 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_007363
Location:INTRON

Gene Symbol:NONO
Accession:NM_001145408
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001786658 CLINVAR
dbSNP (RS) rs2148039353 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NONO CLINVAR
OMIM 300084 CLINVAR