View genomic variant #0000000084

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.173795830A>G
Published as -
GERP 5.370
Segregation -
DB-ID DARS2_000017 See all 2 reported entries
MSCV MSCV_0000084
dbSNP ID rs121918209
Frequency -
Sources ; clinVar; Ensembl;
Reference 17384640
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

3 entries on 1 page. Showing entries 1 - 3.
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 0000000084 +/+ - 2/14 c.133A>G p.(Ser45Gly) - missense_variant - -
DARS2 00000089 XM_005245299.1 0000000084 +/+ - - c.-26A>G p.(=) - - - -
DARS2 00000090 XM_005245300.1 0000000084 +/+ - 2/14 c.133A>G p.(Ser45Gly) - missense_variant - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000001118;
Chromosome 1:173795830..173795830
ClinVar Allele ID 16102
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.173795830A>G
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA251680|OMIM:610956.0007|UniProtKB:Q6PI48#VAR 037015
Gene symbol:Gene id. DARS2:55157
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 121918209
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