View genomic variant #0000004072

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.14710G>A
Published as -
GERP 4.150
Segregation -
DB-ID chrM_000445
MSCV MSCV_0004072
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 0000004072 +?/+? - . . . - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000851099; RCV003153876;
Chromosome M:14710..14710
ClinVar Allele ID 677599
Disease database name and identifier MONDO:MONDO:0044970, MeSH:D028361, MedGen:C0751651, Orphanet:68380|MONDO:MONDO:0010789, MedGen:C0162671, OMIM:540000, Orphanet:550
ClinVar preferred disease name Mitochondrial disease|Juvenile myopathy, encephalopathy, lactic acidosis AND stroke
HGVS variant names NC 012920.1:m.14710G>A
ClinVar review status reviewed by expert panel
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported Genetic Testing Registry (GTR):GTR000591967|Genetic Testing Registry (GTR):GTR000591975|Genetic Testing Registry (GTR):GTR000591976
Gene symbol:Gene id. MT-TE:4556
Allele origin germline
dbSNP ID 1603224840
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-TEEncephalomyopathy + RetinopathyG14710AtRNA Glu-+ReportedRNA

Ensembl Variant Phenotype Information:

None