View genomic variant #0000000098

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.173826730C>T
Published as -
GERP 4.730
Segregation -
DB-ID DARS2_000006 See all 2 reported entries
MSCV MSCV_0000098
dbSNP ID rs200670286
Frequency -
Sources ; clinVar;
Reference 21749991
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

2 entries on 1 page. Showing entries 1 - 2.
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 0000000098 +/+ - 17/17 c.1825C>T p.(Arg609Trp) possibly_damaging(0.773) missense_variant - deleterious(0)
DARS2 00000089 XM_005245299.1 0000000098 +/+ - 16/16 c.1600C>T p.(Arg534Trp) - missense_variant - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000023848; RCV001762056;
Chromosome 1:173826730..173826730
Allele frequencies from ExAC 0.00001
ClinVar Allele ID 39820
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.173826730C>T
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
Variant clinical sources reported ClinGen:CA259925|OMIM:610956.0013
Gene symbol:Gene id. DARS2:55157
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 200670286
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