View genomic variant #0000025771

Chromosome 2
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.84686354T>A
Published as -
GERP -
Segregation -
DB-ID SUCLG1_000040
MSCV -
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 Lishuang Shen




Variant on transcripts

1 entry on 1 page. Showing entry 1.
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Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
SUCLG1 00000316 NM_003849.3 0000025771 ./. - - c.40A>T p.(Met14Leu) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000680168;
Chromosome 2:84686354..84686354
ClinVar Allele ID 552068
Disease database name and identifier MONDO:MONDO:0009504, MedGen:C3151476, OMIM:245400, Orphanet:17
ClinVar preferred disease name Mitochondrial DNA depletion syndrome 9
HGVS variant names NC 000002.11:g.84686354T>A
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Pathogenic(1)|Uncertain significance(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. SUCLG1:8802
Molecular consequence SO:0001583|missense variant
Allele origin
dbSNP ID 796052053
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000186203; RCV002517830; RCV003137762;
Chromosome 2:84686354..84686354
ClinVar Allele ID 200028
Disease database name and identifier MeSH:D030342, MedGen:C0950123|MedGen:CN517202|MONDO:MONDO:0009504, MedGen:C3151476, OMIM:245400, Orphanet:17
ClinVar preferred disease name Inborn genetic diseases|not provided|Mitochondrial DNA depletion syndrome 9
HGVS variant names NC 000002.11:g.84686354T>C
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA313064
Gene symbol:Gene id. SUCLG1:8802
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 796052053
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