View genomic variant #0000019231

Chromosome 2
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.74184243del
Published as -
GERP -
Segregation -
DB-ID DGUOK_000015
MSCV MSCV_0019231
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00016 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 0000019231 ./. - - c.592-9del p.(=) - - - -
DGUOK 00003342 NM_080916.2 0000019231 ./. - - c.592-9del p.(=) - - - -
DGUOK 00000093 NM_080918.1 0000019231 ./. - - c.444-1030del p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000335890; RCV002057710;
Chromosome 2:74184243..74184243
Allele frequencies from ESP 0.00016
Allele frequencies from ExAC 0.00008
ClinVar Allele ID 287252
Disease database name and identifier MONDO:MONDO:0018158, MedGen:C0342782, OMIM:PS603041, Orphanet:35698|MedGen:CN517202
ClinVar preferred disease name Mitochondrial DNA depletion syndrome|not provided
HGVS variant names NC 000002.11:g.74184243del
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(1)|Likely benign(1)
Variant type Deletion
Sequence Ontology for variant type SO:0000159
Variant clinical sources reported ClinGen:CA1718305
Gene symbol:Gene id. DGUOK:1716
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 749290011
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