RGD:12840621 Rat Genome Database

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Variant: RGD:12840621 -  Homo sapiens

RGD ID: 12840621
RS ID: rs377245940
ClinVar ID: CV377858
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC112552175  NDUFA11  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 19 5,903,762
GRCh38 19 5,903,751
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.5263C>T
NC_000019.10:g.5903751G>A
NC_000019.9:g.5903762G>A
NM_175614.2:c.-43C>T
More... 		12/27/2017 5 prime utr variant likely benign AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:NDUFA11
Accession:NM_175614
Location:5UTRS;EXON

Gene Symbol:NDUFA11
Accession:NM_001193375
Location:5UTRS;EXON

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000431062 CLINVAR
dbSNP (RS) rs377245940 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene 112552175 CLINVAR
  NDUFA11 CLINVAR
OMIM 612638 CLINVAR