View genomic variant #0000023779

Chromosome 1
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.150461502G>A
Published as -
GERP -
Segregation -
DB-ID TARS2_000003
MSCV -
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 Lishuang Shen




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     
TARS2 00001213 NM_001271895.1 0000023779 ./. - - c.326G>A p.(Arg109Gln) - - - -
TARS2 00001214 NM_001271896.1 0000023779 ./. - - c.326G>A p.(Arg109Gln) - - - -
TARS2 00001212 NM_025150.4 0000023779 ./. - - c.326G>A p.(Arg109Gln) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000761523; RCV002533868;
Chromosome 1:150461502..150461502
Allele frequencies from ExAC 0.00002
ClinVar Allele ID 612252
Disease database name and identifier MONDO:MONDO:0014398, MedGen:C4706316, OMIM:615918, Orphanet:420733|MeSH:D030342, MedGen:C0950123
ClinVar preferred disease name Combined oxidative phosphorylation defect type 21|Inborn genetic diseases
HGVS variant names NC 000001.10:g.150461502G>A
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. TARS2:80222
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant
Allele origin germline
dbSNP ID 760526545
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