View genomic variant #0000018390

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.17924535C>A
Published as -
GERP -
Segregation -
DB-ID ATPAF2_000003
MSCV MSCV_0018390
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

2 entries on 1 page. Showing entries 1 - 2.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
ATPAF2 00000547 NM_145691.3 0000018390 ./. - - c.634G>T p.(Ala212Ser) - - - -
ATPAF2 00000548 XM_005256848.1 0000018390 ./. - - c.634G>T p.(Ala212Ser) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000384895; RCV002274015;
Chromosome 17:17924535..17924535
Allele frequencies from ExAC 0.00034
Allele frequencies from TGP 0.00080
ClinVar Allele ID 337355
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0011421, MedGen:C3276276, OMIM:604273, Orphanet:254913
ClinVar preferred disease name not provided|Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1
HGVS variant names NC 000017.10:g.17924535C>A
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(2)|Likely benign(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA8421785
Gene symbol:Gene id. ATPAF2:91647
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 141020107
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