View genomic variant #0000001506

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.14846G>A
Published as -
GERP 4.150
Segregation -
DB-ID chrM_000043 See all 4 reported entries
MSCV MSCV_0001506
dbSNP ID rs207459998
Frequency -
Sources ; clinVar; Mitomap; Ensembl;
Reference 10502593
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 0000001506 +/+ - . c.100G>A p.G34S - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000010317; RCV000855169; RCV002265553;
Chromosome M:14846..14846
ClinVar Allele ID 24718
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 MT-CYB associated Exercise intolerance|MT-CYB associated Mitochondrial myopathy|Exercise intolerance|Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
HGVS variant names NC 012920.1:m.14846G>A
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic/Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA120617|OMIM:516020.0006
Gene symbol:Gene id. MT-CYB:4519
Allele origin
dbSNP ID 207459998
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-CYBEXITG14846AG-S-+ReportedCoding_and_Control_Region

Ensembl Variant Phenotype Information:

None