RGD:12835429 Rat Genome Database

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Variant: RGD:12835429 -  Homo sapiens

RGD ID: 12835429
RS ID: rs758297555
ClinVar ID: CV379668
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NDUFA11  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 19 5,897,022
GRCh38 19 5,897,011
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_027808.1:g.12003C>T
NC_000019.10:g.5897011G>A
NC_000019.9:g.5897022G>A
NM_175614.2:c.98-14C>T
More...
08/05/2016 intron variant likely benign AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:NDUFA11
Accession:NM_001193375
Location:INTRON

Gene Symbol:NDUFA11
Accession:NM_175614
Location:INTRON

Gene Symbol:NDUFA11
Accession:NR_034166
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000421653 CLINVAR
dbSNP (RS) rs758297555 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene NDUFA11 CLINVAR
OMIM 612638 CLINVAR