View genomic variant #0000001477

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.12338T>C
Published as -
GERP 3.280
Segregation -
DB-ID chrM_000157 See all 2 reported entries
MSCV MSCV_0001477
dbSNP ID rs201863060
Frequency -
Sources ; clinVar; Mitomap;
Reference 21131053
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-ND5 00001347 MT-ND5-201 0000001477 +/+ - . c.2T>C p.M1T - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000022893; RCV000854787;
Chromosome M:12338..12338
ClinVar Allele ID 38954
Disease database name and identifier MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506|Human Phenotype Ontology:HP:0001086, Human Phenotype Ontology:HP:0001112, MONDO:MONDO:0010788, MedGen:C0917796, OMIM:535000, Orphanet:104
ClinVar preferred disease name Leigh syndrome|Leber optic atrophy
HGVS variant names NC 012920.1:m.12338T>C
ClinVar review status criteria provided, single submitter
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA259737|OMIM:516005.0011
Gene symbol:Gene id. MT-ND5:4540
Allele origin germline
dbSNP ID 201863060
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-ND5DEAF1555 increased penetrance / LHONT12338CM-T+-Conflicting reportsCoding_and_Control_Region

Ensembl Variant Phenotype Information:

None