View genomic variant #0000019697

Chromosome 2
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.240954286T>C
Published as -
GERP -
Segregation -
DB-ID NDUFA10_000036
MSCV MSCV_0019697
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.002 View details
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     
NDUFA10 00000183 NM_004544.3 0000019697 ./. - - c.548-9A>G p.(=) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000127100; RCV000275112; RCV000355965; RCV000676557;
Chromosome 2:240954286..240954286
Allele frequencies from ESP 0.00200
Allele frequencies from ExAC 0.00163
Allele frequencies from TGP 0.00200
ClinVar Allele ID 142139
Disease database name and identifier MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506|MONDO:MONDO:0100224, MedGen:CN257533, OMIM:252010|MedGen:C3661900|MedGen:CN169374
ClinVar preferred disease name Leigh syndrome|Mitochondrial complex I deficiency, nuclear type 1|not provided|not specified
HGVS variant names NC 000002.11:g.240954286T>C
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(2)|Benign(2)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA292420
Gene symbol:Gene id. NDUFA10:4705
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 147876332
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