View genomic variant #0000000091

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.173802608A>G
Published as -
GERP 3.590
Segregation -
DB-ID DARS2_000016 See all 2 reported entries
MSCV MSCV_0000091
dbSNP ID rs35515638
Frequency -
Sources ; clinVar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.02883 View details
Owner LOVD




Variant on transcripts

3 entries on 1 page. Showing entries 1 - 3.
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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 0000000091 -/- - 6/17 c.587A>G p.(Lys196Arg) benign(0.012) missense_variant - tolerated(0.28)
DARS2 00000089 XM_005245299.1 0000000091 -/- - 5/16 c.362A>G p.(Lys121Arg) - missense_variant - -
DARS2 00000090 XM_005245300.1 0000000091 -/- - 6/17 c.587A>G p.(Lys196Arg) benign(0.012) missense_variant - tolerated(0.28)
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000124662; RCV000291422; RCV000676394;
Chromosome 1:173802608..173802608
Allele frequencies from ESP 0.02883
Allele frequencies from ExAC 0.00745
Allele frequencies from TGP 0.02416
ClinVar Allele ID 34399
Disease database name and identifier MONDO:MONDO:0012622, MedGen:C1970180, OMIM:611105, Orphanet:137898|MedGen:CN169374|MedGen:C3661900
ClinVar preferred disease name Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome|not specified|not provided
HGVS variant names NC 000001.10:g.173802608A>G
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA290571|UniProtKB:Q6PI48#VAR 034525
Gene symbol:Gene id. DARS2:55157
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 35515638
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