RGD:14744577 Rat Genome Database

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Variant: RGD:14744577 -  Homo sapiens

RGD ID: 14744577
RS ID: rs2286978
ClinVar ID: CV662146
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NDUFA4  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 7 10,978,789
GRCh38 7 10,939,162
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_002489.4:c.43-266T>A
NG_050627.1:g.6025T>A
NC_000007.14:g.10939162A>T
NC_000007.13:g.10978789A>T
More... 		06/14/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:NDUFA4
Accession:NM_002489
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000842848 CLINVAR
dbSNP (RS) rs2286978 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NDUFA4 CLINVAR
OMIM 603833 CLINVAR