View genomic variant #0000019664

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.240898578C>T
Published as -
GERP -
Segregation -
DB-ID NDUFA10_000057
MSCV MSCV_0019664
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.
Legend  

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 0000019664 ./. - - c.*1957G>A p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000300653; RCV000353226; RCV001709606;
Chromosome 2:240898578..240898578
Allele frequencies from TGP 0.50839
ClinVar Allele ID 288875
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0100224, MedGen:CN257533, OMIM:252010|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name not provided|Mitochondrial complex I deficiency, nuclear type 1|Leigh syndrome
HGVS variant names NC 000002.11:g.240898578C>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA10614942
Gene symbol:Gene id. NDUFA10:4705
Molecular consequence SO:0001619|non-coding transcript variant, SO:0001624|3 prime UTR variant
Allele origin germline
dbSNP ID 4854069
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