View genomic variant #0000001543

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.119005968G>C
Published as -
GERP 3.790
Segregation -
DB-ID NDUFA1_000001 See all 2 reported entries
MSCV MSCV_0001543
dbSNP ID rs1801316
Frequency -
Sources ; clinvar;
Reference 19185523;21596602
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00672 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     
NDUFA1 00000182 NM_004541.3 0000001543 +/+ - 1/3 c.94G>C p.(=) probably_damaging(0.998) missense_variant - tolerated(0.1)
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000030653; RCV000173348; RCV000418299; RCV000990934; RCV002313724;
Chromosome X:119005968..119005968
Allele frequencies from ESP 0.00672
Allele frequencies from TGP 0.00079
ClinVar Allele ID 45630
Disease database name and identifier MedGen:CN169374|MONDO:MONDO:0026720, MedGen:C4746984, OMIM:301020|MeSH:D030342, MedGen:C0950123|MedGen:C3661900|MONDO:MONDO:0100133, MedGen:C1838979, Orphanet:2609
ClinVar preferred disease name not specified|Mitochondrial complex 1 deficiency, nuclear type 12|Inborn genetic diseases|not provided|Mitochondrial complex I deficiency
HGVS variant names NC 000023.10:g.119005968G>C
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign/Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA090926|OMIM:300078.0003|UniProtKB:O15239#VAR 014485
Gene symbol:Gene id. NDUFA1:4694|LOC130068621:130068621
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 1801316
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