View genomic variant #0000024779

Chromosome 13
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.48528575G>A
Published as -
GERP -
Segregation -
DB-ID SUCLA2_000045
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

4 entries on 1 page. Showing entries 1 - 4.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
SUCLA2 00000313 NM_003850.2 0000024779 ./. - - c.920C>T p.(Ala307Val) - - - -
SUCLA2 00000312 XM_005266579.1 0000024779 ./. - - c.746C>T - - - - -
SUCLA2 00000315 XM_005266580.1 0000024779 ./. - - c.746C>T - - - - -
SUCLA2 00000314 XM_005266581.1 0000024779 ./. - - c.518C>T p.(Ala173Val) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000761522; RCV003396328;
Chromosome 13:48528575..48528575
ClinVar Allele ID 612302
Disease database name and identifier .|MONDO:MONDO:0012791, MedGen:C2749864, OMIM:612073, Orphanet:1933
ClinVar preferred disease name SUCLA2-related condition|Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria
HGVS variant names NC 000013.10:g.48528575G>A
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Likely pathogenic(2)|Uncertain significance(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. SUCLA2:8803
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 1011464708
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