View genomic variant #0000019264

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.84652653G>A
Published as -
GERP -
Segregation -
DB-ID SUCLG1_000027
MSCV MSCV_0019264
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00215 View details
Owner LOVD




Variant on transcripts

1 entry on 1 page. Showing entry 1.
Legend  

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 0000019264 ./. - - c.900C>T p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000186192; RCV000279864; RCV000316302; RCV000677031;
Chromosome 2:84652653..84652653
Allele frequencies from ESP 0.00215
Allele frequencies from ExAC 0.00127
Allele frequencies from TGP 0.00040
ClinVar Allele ID 200016
Disease database name and identifier MONDO:MONDO:0018158, MedGen:C0342782, OMIM:PS603041, Orphanet:35698|MedGen:CN169374|MedGen:C3661900|MONDO:MONDO:0009504, MedGen:C3151476, OMIM:245400, Orphanet:17
ClinVar preferred disease name Mitochondrial DNA depletion syndrome|not specified|not provided|Mitochondrial DNA depletion syndrome 9
HGVS variant names NC 000002.11:g.84652653G>A
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(2)|Benign(2)|Likely benign(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA313042
Gene symbol:Gene id. SUCLG1:8802
Molecular consequence SO:0001819|synonymous variant
Allele origin germline
dbSNP ID 113840224
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