View genomic variant #0000017289

Chromosome 13
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.48528283C>T
Published as -
GERP -
Segregation -
DB-ID SUCLA2_000013
MSCV MSCV_0017289
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00085 View details
Owner LOVD




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 0000017289 ./. - - c.1099G>A p.(Asp367Asn) - - - -
SUCLA2 00000312 XM_005266579.1 0000017289 ./. - - c.925G>A - - - - -
SUCLA2 00000315 XM_005266580.1 0000017289 ./. - - c.925G>A - - - - -
SUCLA2 00000314 XM_005266581.1 0000017289 ./. - - c.697G>A p.(Asp233Asn) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV003029192;
Chromosome 13:48528283..48528283
ClinVar Allele ID 2166572
Disease database name and identifier MONDO:MONDO:0012791, MedGen:C2749864, OMIM:612073, Orphanet:1933
ClinVar preferred disease name Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria
HGVS variant names NC 000013.10:g.48528283C>A
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
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
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000128329; RCV000676872; RCV000999962;
Chromosome 13:48528283..48528283
Allele frequencies from ESP 0.00085
Allele frequencies from ExAC 0.01337
Allele frequencies from TGP 0.02296
ClinVar Allele ID 143065
Disease database name and identifier MedGen:CN169374|MedGen:C3661900|MONDO:MONDO:0012791, MedGen:C2749864, OMIM:612073, Orphanet:1933
ClinVar preferred disease name not specified|not provided|Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria
HGVS variant names NC 000013.10:g.48528283C>T
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:CA293807
Gene symbol:Gene id. SUCLA2:8803
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 117412559
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