View genomic variant #0000000092

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.173807344C>T
Published as -
GERP 4.760
Segregation -
DB-ID DARS2_000001 See all 2 reported entries
MSCV MSCV_0000092
dbSNP ID rs121918206
Frequency -
Sources ; clinVar; Ensembl;
Reference 17384640
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 0000000092 +/+ - 9/17 c.787C>T p.(Arg263*) - stop_gained - -
DARS2 00000089 XM_005245299.1 0000000092 +/+ - 8/16 c.562C>T p.(Arg188*) - stop_gained - -
DARS2 00000090 XM_005245300.1 0000000092 +/+ - 9/17 c.787C>T p.(Arg263*) - stop_gained - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000001114; RCV002512634;
Chromosome 1:173807344..173807344
ClinVar Allele ID 16098
Disease database name and identifier MedGen:CN517202|MONDO:MONDO:0012622, MedGen:C1970180, OMIM:611105, Orphanet:137898
ClinVar preferred disease name not provided|Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome
HGVS variant names NC 000001.10:g.173807344C>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA251677|OMIM:610956.0003
Gene symbol:Gene id. DARS2:55157
Molecular consequence SO:0001587|nonsense
Allele origin germline
dbSNP ID 121918206
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