View genomic variant #0000001517

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.15812G>A
Published as -
GERP -2.890
Segregation -
DB-ID chrM_000172 See all 2 reported entries
MSCV MSCV_0001517
dbSNP ID rs200336777
Frequency -
Sources ; clinVar; Mitomap; Ensembl;
Reference 1732158;1764087
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 0000001517 +/+ - . c.1066G>A p.V356M - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000010313; RCV000855379;
Chromosome M:15812..15812
ClinVar Allele ID 24714
Disease database name and identifier Human Phenotype Ontology:HP:0001086, Human Phenotype Ontology:HP:0001112, MONDO:MONDO:0010788, MedGen:C0917796, OMIM:535000, Orphanet:104|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name Leber optic atrophy|Leigh syndrome
HGVS variant names NC 012920.1:m.15812G>A
ClinVar review status criteria provided, single submitter
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA254852|OMIM:516020.0002
Gene symbol:Gene id. MT-CYB:4519
Allele origin germline
dbSNP ID 200336777
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-CYBLHONG15812AV-M+-SecondaryCoding_and_Control_Region

Ensembl Variant Phenotype Information:

None