View genomic variant #0000000528

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.48542781C>T
Published as -
GERP 5.980
Segregation -
DB-ID SUCLA2_000003 See all 2 reported entries
MSCV MSCV_0000528
dbSNP ID rs397515462
Frequency -
Sources ; clinvar; ensembl;
Reference 23759946
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 0000000528 +/+ - 6/11 c.751G>A p.(Asp251Asn) possibly_damaging(0.875) missense_variant - deleterious(0)
SUCLA2 00000312 XM_005266579.1 0000000528 +/+ - 6/11 c.577G>A - possibly_damaging(0.875) missense_variant - deleterious(0)
SUCLA2 00000315 XM_005266580.1 0000000528 +/+ - 6/11 c.577G>A - possibly_damaging(0.875) missense_variant - deleterious(0)
SUCLA2 00000314 XM_005266581.1 0000000528 +/+ - 7/12 c.349G>A p.(Asp117Asn) possibly_damaging(0.875) missense_variant - deleterious(0)
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000056273;
Chromosome 13:48542781..48542781
ClinVar Allele ID 76940
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.48542781C>T
ClinVar review status criteria provided, single submitter
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA264788|OMIM:603921.0005|UniProtKB:Q9P2R7#VAR 070123
Gene symbol:Gene id. SUCLA2:8803
Molecular consequence SO:0001583|missense variant
Allele origin
dbSNP ID 397515462
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