View genomic variant #0000017313

Chromosome 13
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.48575385G>A
Published as -
GERP -
Segregation -
DB-ID SUCLA2_000029
MSCV MSCV_0017313
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00015 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 0000017313 ./. - - c.21C>T p.(=) - - - -
SUCLA2 00000312 XM_005266579.1 0000017313 ./. - - c.-84-4227C>T - - - - -
SUCLA2 00000315 XM_005266580.1 0000017313 ./. - - c.-445C>T - - - - -
SUCLA2 00000314 XM_005266581.1 0000017313 ./. - - c.-479C>T p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000381401; RCV001718638;
Chromosome 13:48575385..48575385
Allele frequencies from ESP 0.00015
Allele frequencies from ExAC 0.00005
ClinVar Allele ID 336775
Disease database name and identifier MONDO:MONDO:0012791, MedGen:C2749864, OMIM:612073, Orphanet:1933|MedGen:C3661900
ClinVar preferred disease name Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria|not provided
HGVS variant names NC 000013.10:g.48575385G>A
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(1)|Likely benign(3)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA6978131
Gene symbol:Gene id. SUCLA2:8803
Molecular consequence SO:0001819|synonymous variant
Allele origin germline
dbSNP ID 374479008
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV003055458;
Chromosome 13:48575385..48575385
ClinVar Allele ID 2174894
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.48575385G>C
ClinVar review status criteria provided, single submitter
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. SUCLA2:8803
Molecular consequence SO:0001587|nonsense
Allele origin germline
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