View genomic variant #0000019690

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.240900606G>C
Published as -
GERP -
Segregation -
DB-ID NDUFA10_000027
MSCV MSCV_0019690
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     
NDUFA10 00000183 NM_004544.3 0000019690 ./. - - c.1000-3C>G p.? - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000199808; RCV000333603; RCV000388170;
Chromosome 2:240900606..240900606
Allele frequencies from ExAC 0.00002
ClinVar Allele ID 210796
Disease database name and identifier MONDO:MONDO:0100224, MedGen:CN257533, OMIM:252010|MedGen:CN517202|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 000002.11:g.240900606G>C
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Likely pathogenic(1)|Uncertain significance(2)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA324354
Gene symbol:Gene id. NDUFA10:4705
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 199648872
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