View genomic variant #0000015509

Chromosome 1
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.119619021_119619023del
Published as -
GERP -
Segregation -
DB-ID WARS2_000001
MSCV MSCV_0015509
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

5 entries on 1 page. Showing entries 1 - 5.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
WARS2 00001295 NM_015836.3 0000015509 ./. - - c.298_300del p.(Leu100del) - - - -
WARS2 00001296 NM_201263.2 0000015509 ./. - - c.298_300del p.(Leu100del) - - - -
WARS2 00001297 XM_005270350.1 0000015509 ./. - - c.244_246del p.(Leu82del) - - - -
WARS2 00001294 XM_005270351.1 0000015509 ./. - - c.177+121_177+123del p.(=) - - - -
WARS2 00001293 XM_005270352.1 0000015509 ./. - - c.298_300del p.(Leu100del) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000509070; RCV000623999; RCV001836832;
Chromosome 1:119619021..119619023
ClinVar Allele ID 434544
Disease database name and identifier MONDO:MONDO:0030676, MedGen:C5676913, OMIM:619738|MONDO:MONDO:0060578, MedGen:C4540192, OMIM:617710, Orphanet:572798|MeSH:D030342, MedGen:C0950123
ClinVar preferred disease name Parkinsonism-dystonia 3, childhood-onset|Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures|Inborn genetic diseases
HGVS variant names NC 000001.10:g.119619023GAA[1]
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Pathogenic(1)|Uncertain significance(1)
Variant type Microsatellite
Sequence Ontology for variant type SO:0000289
Variant clinical sources reported ClinGen:CA1035365|OMIM:604733.0004
Gene symbol:Gene id. WARS2:10352
Molecular consequence SO:0001627|intron variant, SO:0001822|inframe deletion
Allele origin
dbSNP ID 772867219
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