View genomic variant #0000019228

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.74177730T>A
Published as -
GERP -
Segregation -
DB-ID DGUOK_000012
MSCV MSCV_0019228
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00038 View details
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 0000019228 ./. - - c.462T>A p.(Asn154Lys) - - - -
DGUOK 00003342 NM_080916.2 0000019228 ./. - - c.462T>A p.(Asn154Lys) - - - -
DGUOK 00000093 NM_080918.1 0000019228 ./. - - c.443+3697T>A p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000195764; RCV000239593; RCV003235120; RCV002517206;
Chromosome 2:74177730..74177730
Allele frequencies from ESP 0.00038
Allele frequencies from ExAC 0.00012
Allele frequencies from TGP 0.00020
ClinVar Allele ID 210896
Disease database name and identifier MONDO:MONDO:0014899, MedGen:C4310733, OMIM:617070, Orphanet:329314|MeSH:D030342, MedGen:C0950123|MONDO:MONDO:0009636, MedGen:C5191055, OMIM:251880, Orphanet:279934|MedGen:C3661900
ClinVar preferred disease name Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency|Inborn genetic diseases|Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)|not provided
HGVS variant names NC 000002.11:g.74177730T>A
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Pathogenic(3)|Likely pathogenic(3)|Uncertain significance(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA320135|OMIM:601465.0010|UniProtKB:Q16854#VAR 076981
Gene symbol:Gene id. DGUOK:1716
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant, SO:0001627|intron variant
Allele origin germline
dbSNP ID 144181978
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