View genomic variant #0000015608

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.173794387T>A
Published as -
GERP -
Segregation -
DB-ID DARS2_000040
MSCV MSCV_0015608
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

3 entries on 1 page. Showing entries 1 - 3.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
DARS2 00000091 NM_018122.4 0000015608 ./. - - c.20T>A p.(Leu7*) - - - -
DARS2 00000089 XM_005245299.1 0000015608 ./. - - c.-139T>A p.(=) - - - -
DARS2 00000090 XM_005245300.1 0000015608 ./. - - c.20T>A p.(Leu7*) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000626171;
Chromosome 1:173794387..173794387
ClinVar Allele ID 513498
Disease database name and identifier MONDO:MONDO:0012622, MedGen:C1970180, OMIM:611105, Orphanet:137898
ClinVar preferred disease name Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome
HGVS variant names NC 000001.10:g.173794387T>A
ClinVar review status criteria provided, single submitter
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA343754835
Gene symbol:Gene id. DARS2:55157
Molecular consequence SO:0001587|nonsense
Allele origin inherited
dbSNP ID 1553200766
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