View genomic variant #0000015641

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.173827485C>A
Published as -
GERP -
Segregation -
DB-ID DARS2_000025
MSCV MSCV_0015641
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
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 0000015641 ./. - - c.*642C>A p.(=) - - - -
DARS2 00000089 XM_005245299.1 0000015641 ./. - - c.*642C>A p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000371574;
Chromosome 1:173827485..173827485
Allele frequencies from TGP 0.00938
ClinVar Allele ID 278552
Disease database name and identifier MONDO:MONDO:0012622, MedGen:C1970180, OMIM:611105, Orphanet:137898
ClinVar preferred disease name Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome
HGVS variant names NC 000001.10:g.173827485C>A
ClinVar review status criteria provided, single submitter
Clinical Significance Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA10608813
Gene symbol:Gene id. DARS2:55157
Molecular consequence SO:0001624|3 prime UTR variant
Allele origin germline
dbSNP ID 140743566
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