View genomic variant #0000001435

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.8529G>A
Published as -
GERP 5.070
Segregation -
DB-ID chrM_000052 See all 2 reported entries
MSCV MSCV_0001435
dbSNP ID rs267606881
Frequency -
Sources ; clinVar; Mitomap; Ensembl;
Reference 17954552
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

2 entries on 1 page. Showing entries 1 - 2.
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 0000001435 +/+ - . c.3G>A p.M1M - - - -
MT-ATP8 00001336 MT-ATP8-201 0000001435 +/+ - . c.164G>A p.W55* - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000010271;
Chromosome M:8529..8529
ClinVar Allele ID 24678
Disease database name and identifier MedGen:CN069323
ClinVar preferred disease name Cardiomyopathy, apical hypertrophic, and neuropathy
HGVS variant names NC 012920.1:m.8529G>A
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA120593|OMIM:516070.0002
Gene symbol:Gene id. MT-ATP6:4508|MT-ATP8:4509
Allele origin germline
dbSNP ID 267606881
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-ATP8/6?Apical HCMG8529AW-X (ATP8); M-M (ATP6)+-ReportedCoding_and_Control_Region

Ensembl Variant Phenotype Information:

None