View genomic variant #0000019269

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.84668507G>C
Published as -
GERP -
Segregation -
DB-ID SUCLG1_000030
MSCV MSCV_0019269
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00015 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 0000019269 ./. - - c.395C>G p.(Ala132Gly) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV002651059;
Chromosome 2:84668507..84668507
ClinVar Allele ID 1923831
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.84668507G>A
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
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 germline
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000339430; RCV000396763; RCV003441846;
Chromosome 2:84668507..84668507
Allele frequencies from ESP 0.00015
Allele frequencies from ExAC 0.00016
ClinVar Allele ID 287322
Disease database name and identifier MedGen:C3661900|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.84668507G>C
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:CA1736314
Gene symbol:Gene id. SUCLG1:8802
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 376171433
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