View genomic variant #0000004068

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.14693A>G
Published as -
GERP 1.050
Segregation -
DB-ID chrM_000443
MSCV MSCV_0004068
dbSNP ID -
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-TE 00001349 MT-TE-201 0000004068 +?/+? - . . . - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000851094;
Chromosome M:14693..14693
ClinVar Allele ID 677596
Disease database name and identifier MONDO:MONDO:0010789, MedGen:C0162671, OMIM:540000, Orphanet:550
ClinVar preferred disease name Juvenile myopathy, encephalopathy, lactic acidosis AND stroke
HGVS variant names NC 012920.1:m.14693A>G
ClinVar review status criteria provided, single submitter
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. MT-TE:4556
Allele origin germline
dbSNP ID 386829226
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-TEMELAS/LHON/DEAF/hypertension helperA14693GtRNA Glu++ReportedRNA

Ensembl Variant Phenotype Information:

None