View genomic variant #0000019695

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.240951023G>A
Published as -
GERP -
Segregation -
DB-ID NDUFA10_000034
MSCV MSCV_0019695
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00038 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     

PolyPhen     

GVS function     

Splice distance     

SIFT     
NDUFA10 00000183 NM_004544.3 0000019695 ./. - - c.749+11C>T p.(=) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000305494; RCV000360176; RCV001672578;
Chromosome 2:240951023..240951023
Allele frequencies from ESP 0.00038
Allele frequencies from ExAC 0.00009
ClinVar Allele ID 286190
Disease database name and identifier MONDO:MONDO:0100133, MedGen:C1838979, Orphanet:2609|MedGen:CN517202|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name Mitochondrial complex I deficiency|not provided|Leigh syndrome
HGVS variant names NC 000002.11:g.240951023G>A
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(2)|Likely benign(2)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA2200881
Gene symbol:Gene id. NDUFA10:4705
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 200760509
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