View genomic variant #0000019703

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.240964714G>C
Published as -
GERP -
Segregation -
DB-ID NDUFA10_000003
MSCV MSCV_0019703
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.08367 View details
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 0000019703 ./. - - c.5C>G p.(Ala2Gly) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000328287; RCV000378198; RCV000383086; RCV000676560;
Chromosome 2:240964714..240964714
Allele frequencies from ESP 0.08367
Allele frequencies from ExAC 0.17243
Allele frequencies from TGP 0.10004
ClinVar Allele ID 274971
Disease database name and identifier MedGen:CN169374|MedGen:C3661900|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506|MONDO:MONDO:0100224, MedGen:CN257533, OMIM:252010
ClinVar preferred disease name not specified|not provided|Leigh syndrome|Mitochondrial complex I deficiency, nuclear type 1
HGVS variant names NC 000002.11:g.240964714G>C
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:CA2201190|UniProtKB:O95299#VAR 034149
Gene symbol:Gene id. NDUFA10:4705
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant
Allele origin germline
dbSNP ID 11541494
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