View genomic variant #0000019261

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.84650857del
Published as -
GERP -
Segregation -
DB-ID SUCLG1_000035
MSCV MSCV_0019261
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.02915 View details
Owner LOVD




Variant on transcripts

1 entry on 1 page. Showing entry 1.
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Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

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DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
SUCLG1 00000316 NM_003849.3 0000019261 ./. - - c.*13del p.(=) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000277101; RCV000332189;
Chromosome 2:84650857..84650857
ClinVar Allele ID 288067
Disease database name and identifier MONDO:MONDO:0018158, MedGen:C0342782, OMIM:PS603041, Orphanet:35698|MONDO:MONDO:0009504, MedGen:C3151476, OMIM:245400, Orphanet:17
ClinVar preferred disease name Mitochondrial DNA depletion syndrome|Mitochondrial DNA depletion syndrome 9
HGVS variant names NC 000002.11:g.84650866del
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type Deletion
Sequence Ontology for variant type SO:0000159
Variant clinical sources reported ClinGen:CA1736106
Gene symbol:Gene id. SUCLG1:8802
Molecular consequence SO:0001624|3 prime UTR variant
Allele origin germline
dbSNP ID 527774382
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