View genomic variant #0000018388

Chromosome 17
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.17921733A>G
Published as -
GERP -
Segregation -
DB-ID ATPAF2_000002
MSCV MSCV_0018388
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 0000018388 ./. - - c.*130T>C p.(=) - - - -
ATPAF2 00000548 XM_005256848.1 0000018388 ./. - - c.*2541T>C p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000292533;
Chromosome 17:17921733..17921733
Allele frequencies from TGP 0.01198
ClinVar Allele ID 345129
Disease database name and identifier MONDO:MONDO:0011421, MedGen:C3276276, OMIM:604273, Orphanet:254913
ClinVar preferred disease name Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1
HGVS variant names NC 000017.10:g.17921733A>G
ClinVar review status criteria provided, single submitter
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA10649632
Gene symbol:Gene id. ATPAF2:91647
Molecular consequence SO:0001624|3 prime UTR variant
Allele origin germline
dbSNP ID 117739515
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