View genomic variant #0000019217

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.74166080C>A
Published as -
GERP -
Segregation -
DB-ID DGUOK_000035
MSCV MSCV_0019217
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

3 entries on 1 page. Showing entries 1 - 3.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
DGUOK 00000092 NM_080916.1 0000019217 ./. - - c.186C>A p.(Tyr62*) - - - -
DGUOK 00003342 NM_080916.2 0000019217 ./. - - c.186C>A p.(Tyr62*) - - - -
DGUOK 00000093 NM_080918.1 0000019217 ./. - - c.186C>A p.(Tyr62*) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000239511;
Chromosome 2:74166080..74166080
ClinVar Allele ID 247479
Disease database name and identifier MONDO:MONDO:0014899, MedGen:C4310733, OMIM:617070, Orphanet:329314
ClinVar preferred disease name Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency
HGVS variant names NC 000002.11:g.74166080C>A
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA10586178|OMIM:601465.0014
Gene symbol:Gene id. DGUOK:1716
Molecular consequence SO:0001587|nonsense, SO:0001627|intron variant
Allele origin germline
dbSNP ID 879255617
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