View genomic variant #0000001434

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.8528T>C
Published as -
GERP 5.070
Segregation -
DB-ID chrM_000051 See all 2 reported entries
MSCV MSCV_0001434
dbSNP ID rs387906422
Frequency -
Sources ; clinVar; Mitomap; ensembl;
Reference 19188198
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 0000001434 +/+ - . c.2T>C p.M1T - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000010272; RCV000854219; RCV002260584;
Chromosome M:8528..8528
ClinVar Allele ID 24679
Disease database name and identifier MONDO:MONDO:0044970, MeSH:D028361, MedGen:C0751651, Orphanet:68380|MONDO:MONDO:0010777, MedGen:C2748884, OMIM:500006|Human Phenotype Ontology:HP:0005152, MONDO:MONDO:0010771, MedGen:C1708371, OMIM:500000, Orphanet:137675
ClinVar preferred disease name Mitochondrial disease|Cardiomyopathy, infantile hypertrophic|Histiocytoid cardiomyopathy
HGVS variant names NC 012920.1:m.8528T>C
ClinVar review status reviewed by expert panel
Clinical Significance Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA120595|Genetic Testing Registry (GTR):GTR000591967|Genetic Testing Registry (GTR):GTR000591975|Genetic Testing Registry (GTR):GTR000591976|OMIM:516060.0010|OMIM:516070.0003
Gene symbol:Gene id. MT-ATP6:4508|MT-ATP8:4509
Allele origin germline
dbSNP ID 387906422
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?Infantile cardiomyopathyT8528CW-R (ATP8); M(start)-T (ATP6)++ReportedCoding_and_Control_Region

Ensembl Variant Phenotype Information:

None