View genomic variant #0000019279

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.84676864C>G
Published as -
GERP -
Segregation -
DB-ID SUCLG1_000025
MSCV MSCV_0019279
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 8.0E-5 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     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
SUCLG1 00000316 NM_003849.3 0000019279 ./. - - c.110G>C p.(Gly37Ala) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000186193; RCV000322795; RCV000377493;
Chromosome 2:84676864..84676864
Allele frequencies from ESP 0.00008
Allele frequencies from ExAC 0.00025
ClinVar Allele ID 200027
Disease database name and identifier MedGen:CN517202|MONDO:MONDO:0018158, MedGen:C0342782, OMIM:PS603041, Orphanet:35698|MONDO:MONDO:0009504, MedGen:C3151476, OMIM:245400, Orphanet:17
ClinVar preferred disease name not provided|Mitochondrial DNA depletion syndrome|Mitochondrial DNA depletion syndrome 9
HGVS variant names NC 000002.11:g.84676864C>G
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(3)|Likely benign(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA313044|UniProtKB:P53597#VAR 076432
Gene symbol:Gene id. SUCLG1:8802
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 369610897
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