View genomic variant #0000004933

Chromosome M
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) m.8719G>A
Published as -
GERP 4.900
Segregation -
DB-ID chrM_001335
MSCV MSCV_0004933
dbSNP ID rs28624611
Frequency -
Sources ; Mitomap;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

1 entry on 1 page. Showing entry 1.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
MT-ATP6 00001337 MT-ATP6-201 0000004933 +?/+? - . c.193G>A p.G65* - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000854300;
Chromosome M:8719..8719
ClinVar Allele ID 681497
Disease database name and identifier MONDO:MONDO:0010780, MedGen:C3151898, OMIM:500009, Orphanet:254864
ClinVar preferred disease name Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
HGVS variant names NC 012920.1:m.8719G>A
ClinVar review status criteria provided, single submitter
Clinical Significance Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. MT-ATP6:4508
Allele origin germline
dbSNP ID 28624611
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-ATP6Suspected mito diseaseG8719AG-Ter-+ReportedCoding_and_Control_Region

Ensembl Variant Phenotype Information:

None