View genomic variant #0000000527

Chromosome 13
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.48528645G>A
Published as -
GERP 5.670
Segregation -
DB-ID SUCLA2_000004 See all 2 reported entries
MSCV MSCV_0000527
dbSNP ID rs121908538
Frequency -
Sources ; clinVar; Ensembl;
Reference 17301081
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 8.0E-5 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 0000000527 +/+ - 7/11 c.850C>T p.(Arg284Cys) benign(0.136) missense_variant - deleterious(0)
SUCLA2 00000312 XM_005266579.1 0000000527 +/+ - 7/11 c.676C>T - benign(0.136) missense_variant - deleterious(0)
SUCLA2 00000315 XM_005266580.1 0000000527 +/+ - 7/11 c.676C>T - benign(0.136) missense_variant - deleterious(0)
SUCLA2 00000314 XM_005266581.1 0000000527 +/+ - 8/12 c.448C>T p.(Arg150Cys) benign(0.136) missense_variant - deleterious(0)
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000006344; RCV002293407;
Chromosome 13:48528645..48528645
Allele frequencies from ExAC 0.00002
ClinVar Allele ID 21017
Disease database name and identifier MedGen:CN517202|MONDO:MONDO:0012791, MedGen:C2749864, OMIM:612073, Orphanet:1933
ClinVar preferred disease name not provided|Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria
HGVS variant names NC 000013.10:g.48528645G>A
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic/Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA253672|OMIM:603921.0004|UniProtKB:Q9P2R7#VAR 046216
Gene symbol:Gene id. SUCLA2:8803
Molecular consequence SO:0001583|missense variant
Allele origin
dbSNP ID 121908538
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