View genomic variant #0000001366

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.4300A>G
Published as -
GERP 4.530
Segregation -
DB-ID chrM_000011 See all 2 reported entries
MSCV MSCV_0001366
dbSNP ID rs121434470
Frequency -
Sources ; clinVar; Mitomap; Ensembl;
Reference 12767666
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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MT-TI 00001322 MT-TI-201 0000001366 +/+ - . . . - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000010229; RCV001251031; RCV002247293; RCV002291210;
Chromosome M:4300..4300
ClinVar Allele ID 24645
Disease database name and identifier EFO:EFO 0000407, Human Phenotype Ontology:HP:0001644, Human Phenotype Ontology:HP:0001725, Human Phenotype Ontology:HP:0005159, Human Phenotype Ontology:HP:0200130, MONDO:MONDO:0005021, MeSH:D002311, MedGen:C0007193, Orphanet:217604|Human Phenotype Ontology:HP:0001670, MedGen:C0205700|MONDO:MONDO:0044970, MeSH:D028361, MedGen:C0751651, Orphanet:68380|MONDO:MONDO:0010790, MedGen:C0162672, OMIM:545000, Orphanet:551|MONDO:MONDO:0024573, MeSH:D024741, MedGen:C0949658, OMIM:PS192600, Orphanet:155
ClinVar preferred disease name Primary dilated cardiomyopathy|Asymmetric septal hypertrophy|Mitochondrial disease|MERRF syndrome|Primary familial hypertrophic cardiomyopathy
HGVS variant names NC 012920.1:m.4300A>G
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:CA254842|Genetic Testing Registry (GTR):GTR000591967|Genetic Testing Registry (GTR):GTR000591969|Genetic Testing Registry (GTR):GTR000591975|Genetic Testing Registry (GTR):GTR000591976|OMIM:590045.0006
Gene symbol:Gene id. MT-TI:4565
Allele origin germline
dbSNP ID 121434470
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-TIMICMA4300GtRNA Ile++CfrmRNA

Ensembl Variant Phenotype Information:

None