View genomic variant #0000004641

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.5523T>G
Published as -
GERP 2.760
Segregation -
DB-ID chrM_000304 See all 3 reported entries
MSCV MSCV_0004641
dbSNP ID -
Frequency -
Sources ; Mitomap;
Reference -
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-TW 00001326 MT-TW-201 0000004641 +?/+? - . . . - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000144001;
Chromosome M:5523..5523
ClinVar Allele ID 165631
Disease database name and identifier MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name Leigh syndrome
HGVS variant names NC 012920.1:m.5523T>G
ClinVar review status no assertion provided
Clinical Significance not provided
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA345912
Gene symbol:Gene id. MT-TW:4578
Allele origin germline
dbSNP ID 587776435
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-TWLeigh SyndromeT5523GtRNA Trp-+ReportedRNA

Ensembl Variant Phenotype Information:

None