View genomic variant #0000019275

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.84670490C>T
Published as -
GERP -
Segregation -
DB-ID SUCLG1_000021
MSCV MSCV_0019275
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00108 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 0000019275 ./. - - c.236G>A p.(Gly79Asp) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000239306; RCV000369613; RCV000390394; RCV000428598;
Chromosome 2:84670490..84670490
Allele frequencies from ESP 0.00108
Allele frequencies from ExAC 0.00139
Allele frequencies from TGP 0.00060
ClinVar Allele ID 200025
Disease database name and identifier MONDO:MONDO:0018158, MedGen:C0342782, OMIM:PS603041, Orphanet:35698|MONDO:MONDO:0009504, MedGen:C3151476, OMIM:245400, Orphanet:17|MedGen:CN169374|MedGen:C3661900
ClinVar preferred disease name Mitochondrial DNA depletion syndrome|Mitochondrial DNA depletion syndrome 9|not specified|not provided
HGVS variant names NC 000002.11:g.84670490C>T
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(9)|Likely benign(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA313048
Gene symbol:Gene id. SUCLG1:8802
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 143030960
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