View genomic variant #0000004918

Chromosome M
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type ins
DNA change (genomic) (Relative to hg19 / GRCh37) m.8613_8614insT
Published as -
GERP -
Segregation -
DB-ID chrM_001204
MSCV MSCV_0004918
dbSNP ID rs199476139
Frequency -
Sources ; Ensembl;
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.
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 0000004918 +?/+? - . c.87_88insT p.L30NA - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000854259;
Chromosome M:8612..8612
ClinVar Allele ID 681460
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.8612T>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 1603221635
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None