View genomic variant #0000017314

Chromosome 13
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.48575417A>C
Published as -
GERP -
Segregation -
DB-ID SUCLA2_000030
MSCV MSCV_0017314
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 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 0000017314 ./. - - c.-12T>G p.(=) - - - -
SUCLA2 00000312 XM_005266579.1 0000017314 ./. - - c.-84-4259T>G - - - - -
SUCLA2 00000315 XM_005266580.1 0000017314 ./. - - c.-477T>G - - - - -
SUCLA2 00000314 XM_005266581.1 0000017314 ./. - - c.-511T>G p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000296458;
Chromosome 13:48575417..48575417
Allele frequencies from ExAC 0.00024
ClinVar Allele ID 328426
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.48575417A>C
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA6978142
Gene symbol:Gene id. SUCLA2:8803
Allele origin germline
dbSNP ID 753085253
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000430477;
Chromosome 13:48575417..48575417
ClinVar Allele ID 373549
Disease database name and identifier MedGen:CN169374
ClinVar preferred disease name not specified
HGVS variant names NC 000013.10:g.48575417A>T
ClinVar review status criteria provided, single submitter
Clinical Significance Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA16606723
Gene symbol:Gene id. SUCLA2:8803
Allele origin germline
dbSNP ID 753085253
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