View genomic variant #0000000717

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.17931590A>T
Published as -
GERP 5.450
Segregation -
DB-ID ATPAF2_000001 See all 2 reported entries
MSCV MSCV_0000717
dbSNP ID rs104894554
Frequency -
Sources ; clinVar; Ensembl;
Reference 14757859
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 0000000717 +/+ - 3/8 c.280T>A p.(Trp94Arg) - missense_variant - -
ATPAF2 00000548 XM_005256848.1 0000000717 +/+ - 3/8 c.280T>A p.(Trp94Arg) - missense_variant - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000002072;
Chromosome 17:17931590..17931590
ClinVar Allele ID 17034
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.17931590A>T
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA214921|OMIM:608918.0001|UniProtKB:Q8N5M1#VAR 023386
Gene symbol:Gene id. ATPAF2:91647
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 104894554
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