View genomic variant #0000001516

Chromosome M
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) m.15615G>A
Published as -
GERP 4.010
Segregation -
DB-ID chrM_000171 See all 2 reported entries
MSCV MSCV_0001516
dbSNP ID rs207459997
Frequency -
Sources ; clinVar; Mitomap; Ensembl;
Reference 8186719;10502593;8910895
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.
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Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
MT-CYB 00001350 MT-CYB-201 0000001516 +/+ - . c.869G>A p.G290D - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000010316; RCV000855331;
Chromosome M:15615..15615
ClinVar Allele ID 24717
Disease database name and identifier Human Phenotype Ontology:HP:0003546, MedGen:C0424551|MONDO:MONDO:0010780, MedGen:C3151898, OMIM:500009, Orphanet:254864
ClinVar preferred disease name Exercise intolerance|Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
HGVS variant names NC 012920.1:m.15615G>A
ClinVar review status criteria provided, single submitter
Clinical Significance Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA120616|OMIM:516020.0005
Gene symbol:Gene id. MT-CYB:4519
Allele origin germline
dbSNP ID 207459997
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-CYBEXIT/Antimycin resistanceG15615AG-D-+ReportedCoding_and_Control_Region

Ensembl Variant Phenotype Information:

None