View genomic variant #0000004492

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.3733G>C
Published as -
GERP 4.530
Segregation -
DB-ID chrM_000707
MSCV MSCV_0004492
dbSNP ID rs199476125
Frequency -
Sources ; clinVar; Mitomap; Ensembl;
Reference 20301353;15505787
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-ND1 00001321 MT-ND1-201 0000004492 +/+ - . c.427G>C p.E143Q - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000010389; RCV002221475;
Chromosome M:3733..3733
ClinVar Allele ID 24775
Disease database name and identifier MONDO:MONDO:0044970, MeSH:D028361, MedGen:C0751651, Orphanet:68380|Human Phenotype Ontology:HP:0001086, Human Phenotype Ontology:HP:0001112, MONDO:MONDO:0010788, MedGen:C0917796, OMIM:535000, Orphanet:104
ClinVar preferred disease name Mitochondrial disease|Leber optic atrophy
HGVS variant names NC 012920.1:m.3733G>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 ClinGen:CA340950|Genetic Testing Registry (GTR):GTR000591967|Genetic Testing Registry (GTR):GTR000591975|Genetic Testing Registry (GTR):GTR000591976|OMIM:516000.0015
Gene symbol:Gene id. MT-ND1:4535
Allele origin
dbSNP ID 199476125
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-ND1LHONG3733AE-K++CfrmCoding_and_Control_Region
MT-ND1LHONG3733CE-Q-+ReportedCoding_and_Control_Region

Ensembl Variant Phenotype Information:

None