View genomic variant #0000001503

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.14709T>C
Published as -
GERP 2.100
Segregation -
DB-ID chrM_000040 See all 3 reported entries
MSCV MSCV_0001503
dbSNP ID rs121434453
Frequency -
Sources ; clinVar; Mitomap; Ensembl;
Reference 12393175;7726154;11437868;15048886;7726155;10392369;9353617;4114165
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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DNA change (cDNA)     

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GVS function     

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SIFT     
MT-TE 00001349 MT-TE-201 0000001503 +/+ - . . . - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000010241; RCV000032996; RCV000495337; RCV000851098; RCV001089486;
Chromosome M:14709..14709
ClinVar Allele ID 24656
Disease database name and identifier MONDO:MONDO:0044970, MeSH:D028361, MedGen:C0751651, Orphanet:68380|Human Phenotype Ontology:HP:0003737, Human Phenotype Ontology:HP:0008960, MONDO:MONDO:0009637, MedGen:C0162670, Orphanet:206966|MONDO:MONDO:0010789, MedGen:C0162671, OMIM:540000, Orphanet:550|MedGen:C4016608|MONDO:MONDO:0010785, MedGen:C0342289, OMIM:520000, Orphanet:225
ClinVar preferred disease name Mitochondrial disease|Inborn mitochondrial myopathy|Juvenile myopathy, encephalopathy, lactic acidosis AND stroke|Myopathy, mitochondrial, with diabetes mellitus|Diabetes-deafness syndrome maternally transmitted
HGVS variant names NC 012920.1:m.14709T>C
ClinVar review status reviewed by expert panel
Clinical Significance Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA120580|Genetic Testing Registry (GTR):GTR000591967|Genetic Testing Registry (GTR):GTR000591969|Genetic Testing Registry (GTR):GTR000591975|Genetic Testing Registry (GTR):GTR000591976|OMIM:590025.0001
Gene symbol:Gene id. MT-TE:4556
Allele origin germline
dbSNP ID 121434453
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-TEMM+DMDF / Encephalomyopathy / Dementia+diabetes+ophthalmoplegiaT14709CtRNA Glu++CfrmRNA

Ensembl Variant Phenotype Information:

None