View genomic variant #0000019218

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.74166145del
Published as -
GERP -
Segregation -
DB-ID DGUOK_000036
MSCV MSCV_0019218
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 0000019218 ./. - - c.251del p.(Ala86Profs*13) - - - -
DGUOK 00003342 NM_080916.2 0000019218 ./. - - c.251del p.(Ala86Profs*13) - - - -
DGUOK 00000093 NM_080918.1 0000019218 ./. - - c.251del p.(Ala86Profs*13) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000008631; RCV000726828;
Chromosome 2:74166145..74166145
ClinVar Allele ID 23192
Disease database name and identifier MedGen:CN517202|MONDO:MONDO:0009636, MedGen:C5191055, OMIM:251880, Orphanet:279934
ClinVar preferred disease name not provided|Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)
HGVS variant names NC 000002.11:g.74166149del
ClinVar review status criteria provided, single submitter
Clinical Significance Pathogenic
Variant type Deletion
Sequence Ontology for variant type SO:0000159
Variant clinical sources reported ClinGen:CA10575500|OMIM:601465.0001
Gene symbol:Gene id. DGUOK:1716
Molecular consequence SO:0001589|frameshift variant, SO:0001627|intron variant
Allele origin germline
dbSNP ID 886037613
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