View genomic variant #0000001485

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.13513G>A
Published as -
GERP 4.550
Segregation -
DB-ID chrM_000165 See all 2 reported entries
MSCV MSCV_0001485
dbSNP ID rs267606897
Frequency -
Sources ; clinVar; Mitomap; Ensembl;
Reference 10589546;17400793;12624137;14520659;14730434;16306525;15576045;18332249;9299505
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-ND5 00001347 MT-ND5-201 0000001485 +/+ - . c.1177G>A p.D393N - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000010346; RCV000010345; RCV000144016; RCV000224472; RCV000494941;
Chromosome M:13513..13513
ClinVar Allele ID 24741
Disease database name and identifier MedGen:C1838951|MONDO:MONDO:0044970, MeSH:D028361, MedGen:C0751651, Orphanet:68380|MedGen:C3661900|MONDO:MONDO:0010789, MedGen:C0162671, OMIM:540000, Orphanet:550|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name Leigh syndrome due to mitochondrial complex I deficiency|Mitochondrial disease|not provided|Juvenile myopathy, encephalopathy, lactic acidosis AND stroke|Leigh syndrome
HGVS variant names NC 012920.1:m.13513G>A
ClinVar review status reviewed by expert panel
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA120632|Genetic Testing Registry (GTR):GTR000500597|Genetic Testing Registry (GTR):GTR000556608|Genetic Testing Registry (GTR):GTR000591967|Genetic Testing Registry (GTR):GTR000591969|Genetic Testing Registry (GTR):GTR000591975|Genetic Testing Registry (GTR):GTR000591976|OMIM:516005.0007
Gene symbol:Gene id. MT-ND5:4540
Allele origin
dbSNP ID 267606897
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-ND5Leigh Disease/MELAS/LHON-MELAS Overlap SyndromeG13513AD-N-+CfrmCoding_and_Control_Region

Ensembl Variant Phenotype Information:

None