View genomic variant #0000001515

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.15579A>G
Published as -
GERP 4.290
Segregation -
DB-ID chrM_000170 See all 2 reported entries
MSCV MSCV_0001515
dbSNP ID rs207460002
Frequency -
Sources ; clinVar; Mitomap; Ensembl;
Reference 11601507
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 0000001515 +/+ - . c.833A>G p.T278C - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000010321; RCV000855325; RCV002247306; RCV003153301;
Chromosome M:15579..15579
ClinVar Allele ID 24722
Disease database name and identifier MONDO:MONDO:0044970, MeSH:D028361, MedGen:C0751651, Orphanet:68380|Human Phenotype Ontology:HP:0001086, Human Phenotype Ontology:HP:0001112, MONDO:MONDO:0010788, MedGen:C0917796, OMIM:535000, Orphanet:104|MONDO:MONDO:0010780, MedGen:C3151898, OMIM:500009, Orphanet:254864|MedGen:C0559758
ClinVar preferred disease name Mitochondrial disease|Leber optic atrophy|Mitochondrial myopathy with reversible cytochrome C oxidase deficiency|Multisystem disorder
HGVS variant names NC 012920.1:m.15579A>G
ClinVar review status reviewed by expert panel
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA120621|Genetic Testing Registry (GTR):GTR000591967|Genetic Testing Registry (GTR):GTR000591975|Genetic Testing Registry (GTR):GTR000591976|OMIM:516020.0010
Gene symbol:Gene id. MT-CYB:4519
Allele origin germline
dbSNP ID 207460002
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-CYBMultisystem DisorderA15579GY-C-+ReportedCoding_and_Control_Region

Ensembl Variant Phenotype Information:

None