View genomic variant #0000001456

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.10197G>A
Published as -
GERP 5.070
Segregation -
DB-ID chrM_000073 See all 3 reported entries
MSCV MSCV_0000202
dbSNP ID rs267606891
Frequency -
Sources ; clinVar; Mitomap; Ensembl;
Reference 17413873;17152068;19458970
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-ND3 00001340 MT-ND3-201 0000001456 +/+ - . c.139G>A p.A47T - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000010363; RCV000010362; RCV000144011; RCV000507278; RCV002247309; RCV002285008; RCV002291213;
Chromosome M:10197..10197
ClinVar Allele ID 24754
Disease database name and identifier MONDO:MONDO:0027068, MedGen:C4746992, OMIM:500014|MedGen:CN169374|MedGen:C3661900|MONDO:MONDO:0044970, MeSH:D028361, MedGen:C0751651, Orphanet:68380|MedGen:CN043634|MONDO:MONDO:0010772, MedGen:C1839040, OMIM:500001, Orphanet:99718|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name Mitochondrial complex 1 deficiency, mitochondrial type 1|not specified|not provided|Mitochondrial disease|Mitochondrial DNA-Associated Leigh Syndrome and NARP|Leber optic atrophy and dystonia|Leigh syndrome
HGVS variant names NC 012920.1:m.10197G>A
ClinVar review status reviewed by expert panel
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA120640|Genetic Testing Registry (GTR):GTR000591967|Genetic Testing Registry (GTR):GTR000591969|Genetic Testing Registry (GTR):GTR000591975|Genetic Testing Registry (GTR):GTR000591976|OMIM:516002.0004
Gene symbol:Gene id. MT-ND3:4537
Allele origin
dbSNP ID 267606891
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-ND3Leigh Disease/Dystonia/Stroke/LDYTG10197AA-T++CfrmCoding_and_Control_Region

Ensembl Variant Phenotype Information:

None