View genomic variant #0000015612

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.173797504T>C
Published as -
GERP -
Segregation -
DB-ID DARS2_000043
MSCV MSCV_0015612
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00015 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 0000015612 ./. - - c.261T>C p.(=) - - - -
DARS2 00000089 XM_005245299.1 0000015612 ./. - - c.69+1580T>C p.(=) - - - -
DARS2 00000090 XM_005245300.1 0000015612 ./. - - c.261T>C p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000388121; RCV000935848;
Chromosome 1:173797504..173797504
Allele frequencies from ESP 0.00015
Allele frequencies from ExAC 0.00056
Allele frequencies from TGP 0.00060
ClinVar Allele ID 278577
Disease database name and identifier MONDO:MONDO:0012622, MedGen:C1970180, OMIM:611105, Orphanet:137898|MedGen:C3661900
ClinVar preferred disease name Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome|not provided
HGVS variant names NC 000001.10:g.173797504T>C
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(1)|Benign(1)|Likely benign(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA1250080
Gene symbol:Gene id. DARS2:55157
Molecular consequence SO:0001819|synonymous variant
Allele origin germline
dbSNP ID 182096636
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