View genomic variant #0000016442

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.47600844T>C
Published as -
GERP -
Segregation -
DB-ID NDUFS3_000010
MSCV MSCV_0016442
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

1 entry on 1 page. Showing entry 1.
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Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
NDUFS3 00000211 NM_004551.2 0000016442 ./. - - c.91T>C p.(=) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000301677; RCV000358793; RCV000616791;
Chromosome 11:47600844..47600844
Allele frequencies from ExAC 0.00016
ClinVar Allele ID 328025
Disease database name and identifier MedGen:CN169374|MONDO:MONDO:0100224, MedGen:CN257533, OMIM:252010|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name not specified|Mitochondrial complex I deficiency, nuclear type 1|Leigh syndrome
HGVS variant names NC 000011.9:g.47600844T>C
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(2)|Likely benign(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA5977804
Gene symbol:Gene id. NDUFS3:4722
Molecular consequence SO:0001819|synonymous variant
Allele origin germline
dbSNP ID 770306617
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