View genomic variant #0000016452

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.47605895G>A
Published as -
GERP -
Segregation -
DB-ID NDUFS3_000004
MSCV MSCV_0016452
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 8.0E-5 View details
Owner LOVD




Variant on transcripts

1 entry on 1 page. Showing entry 1.
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Gene     

Transcript ID     

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Variant ID     

Affects function     

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DNA change (cDNA)     

Protein     

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GVS function     

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SIFT     
NDUFS3 00000211 NM_004551.2 0000016452 ./. - - c.657G>A p.(=) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000325919; RCV000382544; RCV002056209;
Chromosome 11:47605895..47605895
Allele frequencies from ESP 0.00008
Allele frequencies from ExAC 0.00028
Allele frequencies from TGP 0.00020
ClinVar Allele ID 326970
Disease database name and identifier MONDO:MONDO:0100224, MedGen:CN257533, OMIM:252010|MedGen:C3661900|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name Mitochondrial complex I deficiency, nuclear type 1|not provided|Leigh syndrome
HGVS variant names NC 000011.9:g.47605895G>A
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(2)|Benign(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA5978068
Gene symbol:Gene id. NDUFS3:4722
Molecular consequence SO:0001819|synonymous variant
Allele origin germline
dbSNP ID 377323760
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None