View genomic variant #0000015511

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.119683231A>C
Published as -
GERP -
Segregation -
DB-ID WARS2_000003
MSCV MSCV_0015511
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00269 View details
Owner LOVD




Variant on transcripts

4 entries on 1 page. Showing entries 1 - 4.
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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 0000015511 ./. - - c.37T>G p.(Trp13Gly) - - - -
WARS2 00001296 NM_201263.2 0000015511 ./. - - c.37T>G p.(Trp13Gly) - - - -
WARS2 00001294 XM_005270351.1 0000015511 ./. - - c.37T>G p.(Trp13Gly) - - - -
WARS2 00001293 XM_005270352.1 0000015511 ./. - - c.37T>G p.(Trp13Gly) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000509078; RCV000894409; RCV001836831; RCV002524935; RCV003235260; RCV003419881;
Chromosome 1:119683231..119683231
Allele frequencies from ESP 0.00269
Allele frequencies from TGP 0.00200
ClinVar Allele ID 434543
Disease database name and identifier MONDO:MONDO:0030676, MedGen:C5676913, OMIM:619738|MONDO:MONDO:0060578, MedGen:C4540192, OMIM:617710, Orphanet:572798|.|.|MedGen:C3661900|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|WARS2-related condition|WARS2-Related Disorders|not provided|Inborn genetic diseases
HGVS variant names NC 000001.10:g.119683231A>C
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Pathogenic(4)|Likely pathogenic(2)|Uncertain significance(5)|Likely benign(2)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA1035414|OMIM:604733.0002
Gene symbol:Gene id. WARS2:10352|WARS2-AS1:101929147|LOC129931299:129931299
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant, SO:0001623|5 prime UTR variant
Allele origin
dbSNP ID 139548132
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV002663605; RCV002663606;
Chromosome 1:119683231..119683231
ClinVar Allele ID 2002800
Disease database name and identifier MedGen:CN517202|MeSH:D030342, MedGen:C0950123
ClinVar preferred disease name not provided|Inborn genetic diseases
HGVS variant names NC 000001.10:g.119683231A>G
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. WARS2:10352|WARS2-AS1:101929147|LOC129931299:129931299
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant, SO:0001623|5 prime UTR variant
Allele origin germline
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