View genomic variant #0000015508

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.119618996del
Published as -
GERP -
Segregation -
DB-ID WARS2_000006
MSCV MSCV_0015508
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 0000015508 ./. - - c.325del p.(Ser109Alafs*15) - - - -
WARS2 00001296 NM_201263.2 0000015508 ./. - - c.325del p.(Ser109Alafs*15) - - - -
WARS2 00001297 XM_005270350.1 0000015508 ./. - - c.271del p.(Ser91Alafs*15) - - - -
WARS2 00001294 XM_005270351.1 0000015508 ./. - - c.177+148del p.(=) - - - -
WARS2 00001293 XM_005270352.1 0000015508 ./. - - c.325del p.(Ser109Alafs*15) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000509073; RCV002527378;
Chromosome 1:119618996..119618996
ClinVar Allele ID 434542
Disease database name and identifier MONDO:MONDO:0060578, MedGen:C4540192, OMIM:617710, Orphanet:572798|MedGen:CN517202
ClinVar preferred disease name Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures|not provided
HGVS variant names NC 000001.10:g.119619001del
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type Deletion
Sequence Ontology for variant type SO:0000159
Variant clinical sources reported ClinGen:CA526250135|OMIM:604733.0001
Gene symbol:Gene id. WARS2:10352
Molecular consequence SO:0001589|frameshift variant, SO:0001627|intron variant
Allele origin germline
dbSNP ID 1253426801
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