View genomic variant #0000004957

Chromosome M
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) m.9035T>C
Published as -
GERP 4.900
Segregation -
DB-ID chrM_001222
MSCV MSCV_0004957
dbSNP ID -
Frequency -
Sources ; Mitomap;
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 0000004957 +?/+? - . c.509T>C p.L170P - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000851177; RCV000854406; RCV001196557; RCV002260672; RCV002249546; RCV002466594;
Chromosome M:9035..9035
ClinVar Allele ID 677959
Disease database name and identifier MONDO:MONDO:0044970, MeSH:D028361, MedGen:C0751651, Orphanet:68380|Human Phenotype Ontology:HP:0001086, Human Phenotype Ontology:HP:0001112, MONDO:MONDO:0010788, MedGen:C0917796, OMIM:535000, Orphanet:104|Human Phenotype Ontology:HP:0001329, Human Phenotype Ontology:HP:0002073, Human Phenotype Ontology:HP:0002496, Human Phenotype Ontology:HP:0007331, MedGen:C0393525|.|.|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name Mitochondrial disease|Leber optic atrophy|Progressive cerebellar ataxia|See cases|MT-ATP6-related primary mitochondrial disease|Leigh syndrome
HGVS variant names NC 012920.1:m.9035T>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 Genetic Testing Registry (GTR):GTR000591967|Genetic Testing Registry (GTR):GTR000591975|Genetic Testing Registry (GTR):GTR000591976
Gene symbol:Gene id. MT-ATP6:4508
Allele origin
dbSNP ID 1603222000
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-ATP6Ataxia syndromesT9035CL-P+-ReportedCoding_and_Control_Region

Ensembl Variant Phenotype Information:

None