View genomic variant #0000001437

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.8851T>C
Published as -
GERP 4.900
Segregation -
DB-ID chrM_000054 See all 2 reported entries
MSCV MSCV_0001437
dbSNP ID rs199476136
Frequency -
Sources ; clinVar; Mitomap; Ensembl;
Reference 8554662
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 0000001437 +/+ - . c.325T>C p.W109R - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000010280; RCV000144005; RCV001268336; RCV001542705; RCV002221472;
Chromosome M:8851..8851
ClinVar Allele ID 24684
Disease database name and identifier MONDO:MONDO:0044970, MeSH:D028361, MedGen:C0751651, Orphanet:68380|MedGen:C3661900|Human Phenotype Ontology:HP:0001086, Human Phenotype Ontology:HP:0001112, MONDO:MONDO:0010788, MedGen:C0917796, OMIM:535000, Orphanet:104|MONDO:MONDO:0010774, MedGen:C1839022, OMIM:500003|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name Mitochondrial disease|not provided|Leber optic atrophy|Striatonigral degeneration, infantile, mitochondrial|Leigh syndrome
HGVS variant names NC 012920.1:m.8851T>C
ClinVar review status reviewed by expert panel
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA120598|Genetic Testing Registry (GTR):GTR000500595|Genetic Testing Registry (GTR):GTR000591967|Genetic Testing Registry (GTR):GTR000591975|Genetic Testing Registry (GTR):GTR000591976|OMIM:516060.0006
Gene symbol:Gene id. MT-ATP6:4508
Allele origin germline
dbSNP ID 199476136
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-ATP6BSNT8851CW-R++ReportedCoding_and_Control_Region

Ensembl Variant Phenotype Information:

None