View genomic variant #0000001444

Chromosome M
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type del
DNA change (genomic) (Relative to hg19 / GRCh37) m.9205_9206del
Published as -
GERP -
Segregation -
DB-ID chrM_000061
MSCV MSCV_0001444
dbSNP ID rs199476137
Frequency -
Sources ; clinVar; Mitomap; Ensembl;
Reference 12915481;8739943
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.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
MT-ATP6 00001337 MT-ATP6-201 0000001444 +/+ - . c.680_680del p.*227NA - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000854475;
Chromosome M:9205..9205
ClinVar Allele ID 681660
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.9205T>C
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. MT-ATP6:4508
Allele origin germline
dbSNP ID 1603222171
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-ATP6Seizures/Lacticacidemia9205del2Ter-M+-ReportedCoding_and_Control_Region

Ensembl Variant Phenotype Information:

None