View genomic variant #0000023773

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.119619004G>A
Published as -
GERP -
Segregation -
DB-ID WARS2_000008
MSCV -
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 Lishuang Shen




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 0000023773 ./. - - c.317C>T p.(Pro106Leu) - - - -
WARS2 00001296 NM_201263.2 0000023773 ./. - - c.317C>T p.(Pro106Leu) - - - -
WARS2 00001297 XM_005270350.1 0000023773 ./. - - c.263C>T p.(Pro88Leu) - - - -
WARS2 00001294 XM_005270351.1 0000023773 ./. - - c.177+140C>T p.(=) - - - -
WARS2 00001293 XM_005270352.1 0000023773 ./. - - c.317C>T p.(Pro106Leu) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000723321;
Chromosome 1:119619004..119619004
Allele frequencies from ExAC 0.00001
ClinVar Allele ID 583074
Disease database name and identifier MONDO:MONDO:0060578, MedGen:C4540192, OMIM:617710, Orphanet:572798
ClinVar preferred disease name Neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures
HGVS variant names NC 000001.10:g.119619004G>A
ClinVar review status no assertion criteria provided
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. WARS2:10352
Molecular consequence SO:0001583|missense variant, SO:0001627|intron variant
Allele origin germline
dbSNP ID 753188889
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV002936415;
Chromosome 1:119619004..119619008
ClinVar Allele ID 2322822
Disease database name and identifier MeSH:D030342, MedGen:C0950123
ClinVar preferred disease name Inborn genetic diseases
HGVS variant names NC 000001.10:g.119619004 119619008delinsC
ClinVar review status criteria provided, single submitter
Clinical Significance Pathogenic
Variant type Indel
Sequence Ontology for variant type SO:1000032
Gene symbol:Gene id. WARS2:10352
Molecular consequence SO:0001589|frameshift variant, SO:0001627|intron 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