View genomic variant #0000019207

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.74153990G>A
Published as -
GERP -
Segregation -
DB-ID DGUOK_000037
MSCV MSCV_0019207
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.05067 View details
Owner LOVD




Variant on transcripts

3 entries on 1 page. Showing entries 1 - 3.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
DGUOK 00000092 NM_080916.1 0000019207 ./. - - c.-48G>A p.(=) - - - -
DGUOK 00003342 NM_080916.2 0000019207 ./. - - c.-48G>A p.(=) - - - -
DGUOK 00000093 NM_080918.1 0000019207 ./. - - c.-48G>A p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000124679; RCV000368338;
Chromosome 2:74153990..74153990
Allele frequencies from ESP 0.05067
Allele frequencies from ExAC 0.01350
Allele frequencies from TGP 0.04353
ClinVar Allele ID 140787
Disease database name and identifier MONDO:MONDO:0018158, MedGen:C0342782, OMIM:PS603041, Orphanet:35698|MedGen:CN169374
ClinVar preferred disease name Mitochondrial DNA depletion syndrome|not specified
HGVS variant names NC 000002.11:g.74153990G>A
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign/Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA290589
Gene symbol:Gene id. DGUOK:1716
Allele origin germline
dbSNP ID 10186730
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