View genomic variant #0000004919

Chromosome M
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) m.8616G>T
Published as -
GERP -7.460
Segregation -
DB-ID chrM_001205 See all 2 reported entries
MSCV MSCV_0004919
dbSNP ID rs41427749
Frequency -
Sources ;
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-ATP6 00001337 MT-ATP6-201 0000004919 ?/? - . c.90G>T p.L30F - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000224510; RCV000854261;
Chromosome M:8616..8616
ClinVar Allele ID 237307
Disease database name and identifier MedGen:CN517202|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name not provided|Leigh syndrome
HGVS variant names NC 012920.1:m.8616G>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign/Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA10581379
Gene symbol:Gene id. MT-ATP6:4508
Allele origin germline
dbSNP ID 41427749
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