View genomic variant #0000015613

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.173800667T>G
Published as -
GERP -
Segregation -
DB-ID DARS2_000044
MSCV MSCV_0015613
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.01938 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 0000015613 ./. - - c.397-6T>G p.(=) - - - -
DARS2 00000089 XM_005245299.1 0000015613 ./. - - c.172-6T>G p.(=) - - - -
DARS2 00000090 XM_005245300.1 0000015613 ./. - - c.397-6T>G p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000124660; RCV000296248; RCV000676392;
Chromosome 1:173800667..173800667
Allele frequencies from ESP 0.01938
Allele frequencies from ExAC 0.01769
Allele frequencies from TGP 0.01018
ClinVar Allele ID 140774
Disease database name and identifier MedGen:CN169374|MedGen:C3661900|MONDO:MONDO:0012622, MedGen:C1970180, OMIM:611105, Orphanet:137898
ClinVar preferred disease name not specified|not provided|Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome
HGVS variant names NC 000001.10:g.173800667T>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:CA290569
Gene symbol:Gene id. DARS2:55157
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 115051769
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