View genomic variant #0000016446

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.47602542T>C
Published as -
GERP -
Segregation -
DB-ID NDUFS3_000007
MSCV MSCV_0016446
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00023 View details
Owner LOVD




Variant on transcripts

1 entry on 1 page. Showing entry 1.
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Variant ID     

Affects function     

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DNA change (cDNA)     

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SIFT     
NDUFS3 00000211 NM_004551.2 0000016446 ./. - - c.381+6T>C p.(=) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000332963; RCV000389911; RCV001374465; RCV001859811;
Chromosome 11:47602542..47602542
Allele frequencies from ESP 0.00023
Allele frequencies from ExAC 0.00008
ClinVar Allele ID 320904
Disease database name and identifier MONDO:MONDO:0032613, MedGen:C4748766, OMIM:618230|MedGen:CN517202|MONDO:MONDO:0100224, MedGen:CN257533, OMIM:252010|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name Mitochondrial complex 1 deficiency, nuclear type 8|not provided|Mitochondrial complex I deficiency, nuclear type 1|Leigh syndrome
HGVS variant names NC 000011.9:g.47602542T>C
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA5977940|OMIM:603846.0004
Gene symbol:Gene id. NDUFS3:4722
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 377579231
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