View genomic variant #0000003859

Chromosome M
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) m.12372G>A
Published as -
GERP -9.070
Segregation -
DB-ID chrM_001269
MSCV MSCV_0003859
dbSNP ID rs2853499
Frequency -
Sources ; Mitomap;
Reference -
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 0000003859 +?/+? - . c.36G>A p.L12L - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000625870; RCV002248828;
Chromosome M:12372..12372
ClinVar Allele ID 513404
Disease database name and identifier MONDO:MONDO:0044970, MeSH:D028361, MedGen:C0751651, Orphanet:68380|MedGen:CN169374
ClinVar preferred disease name Mitochondrial disease|not specified
HGVS variant names NC 012920.1:m.12372G>A
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Likely pathogenic(1)|Benign(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. MT-ND5:4540
Allele origin
dbSNP ID 2853499
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-ND5Altered brain pHG12372Asyn+-ReportedCoding_and_Control_Region

Ensembl Variant Phenotype Information:

None