View genomic variant #0000004115

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.15150G>A
Published as -
GERP 4.150
Segregation -
DB-ID chrM_000815 See all 2 reported entries
MSCV MSCV_0004115
dbSNP ID rs207460000
Frequency -
Sources ; clinVar; Mitomap; Ensembl;
Reference 11464242
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 0000004115 +/+ - . c.404G>A p.W135* - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000010319; RCV000855232; RCV002247305;
Chromosome M:15150..15150
ClinVar Allele ID 24720
Disease database name and identifier Human Phenotype Ontology:HP:0003546, MedGen:C0424551|MONDO:MONDO:0010780, MedGen:C3151898, OMIM:500009, Orphanet:254864|Human Phenotype Ontology:HP:0001086, Human Phenotype Ontology:HP:0001112, MONDO:MONDO:0010788, MedGen:C0917796, OMIM:535000, Orphanet:104
ClinVar preferred disease name Exercise intolerance|Mitochondrial myopathy with reversible cytochrome C oxidase deficiency|Leber optic atrophy
HGVS variant names NC 012920.1:m.15150G>A
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA120619|OMIM:516020.0008
Gene symbol:Gene id. MT-CYB:4519
Allele origin germline
dbSNP ID 207460000
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-CYBEXITG15150AW-Ter-+ReportedCoding_and_Control_Region

Ensembl Variant Phenotype Information:

None