View genomic variant #0000015505

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.119575679T>A
Published as -
GERP -
Segregation -
DB-ID WARS2_000007
MSCV MSCV_0015505
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00023 View details
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 0000015505 ./. - - c.938A>T p.(Lys313Met) - - - -
WARS2 00001296 NM_201263.2 0000015505 ./. - - c.*304A>T p.(=) - - - -
WARS2 00001297 XM_005270350.1 0000015505 ./. - - c.884A>T p.(Lys295Met) - - - -
WARS2 00001294 XM_005270351.1 0000015505 ./. - - c.767A>T p.(Lys256Met) - - - -
WARS2 00001293 XM_005270352.1 0000015505 ./. - - c.*273A>T p.(=) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000509075; RCV000622962; RCV001726205; RCV003323579;
Chromosome 1:119575679..119575679
Allele frequencies from ESP 0.00023
Allele frequencies from ExAC 0.00015
ClinVar Allele ID 434545
Disease database name and identifier MONDO:MONDO:0060578, MedGen:C4540192, OMIM:617710, Orphanet:572798|MeSH:D030342, MedGen:C0950123|MedGen:C3661900|.
ClinVar preferred disease name Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures|Inborn genetic diseases|not provided|WARS2-Related Disorders
HGVS variant names NC 000001.10:g.119575679T>A
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Pathogenic(2)|Likely pathogenic(2)|Uncertain significance(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA1035179|OMIM:604733.0003
Gene symbol:Gene id. WARS2:10352
Molecular consequence SO:0001583|missense variant, SO:0001624|3 prime UTR variant
Allele origin germline
dbSNP ID 145867327
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