View genomic variant #0000018389

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.17921995C>T
Published as -
GERP -
Segregation -
DB-ID ATPAF2_000017
MSCV MSCV_0018389
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.02399 View details
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 0000018389 ./. - - c.738G>A p.(=) - - - -
ATPAF2 00000548 XM_005256848.1 0000018389 ./. - - c.*2279G>A p.(=) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000123785; RCV000676250; RCV000999963;
Chromosome 17:17921995..17921995
Allele frequencies from ESP 0.02399
Allele frequencies from ExAC 0.03079
Allele frequencies from TGP 0.01637
ClinVar Allele ID 140171
Disease database name and identifier MedGen:CN169374|MedGen:C3661900|MONDO:MONDO:0011421, MedGen:C3276276, OMIM:604273, Orphanet:254913
ClinVar preferred disease name not specified|not provided|Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1
HGVS variant names NC 000017.10:g.17921995C>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA289606
Gene symbol:Gene id. ATPAF2:91647
Molecular consequence SO:0001819|synonymous variant
Allele origin germline
dbSNP ID 33997182
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