View genomic variant #0000004978

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.9191T>C
Published as -
GERP 4.970
Segregation -
DB-ID chrM_000981 See all 3 reported entries
MSCV MSCV_0004978
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 0000004978 +?/+? - . c.665T>C p.L222P - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000144006; RCV002221481;
Chromosome M:9191..9191
ClinVar Allele ID 48652
Disease database name and identifier MONDO:MONDO:0044970, MeSH:D028361, MedGen:C0751651, Orphanet:68380|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name Mitochondrial disease|Leigh syndrome
HGVS variant names NC 012920.1:m.9191T>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:CA345914|Genetic Testing Registry (GTR):GTR000500595
Gene symbol:Gene id. MT-ATP6:4508
Allele origin germline
dbSNP ID 1556423632
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-ATP6Leigh DiseaseT9191CL-P-+ReportedCoding_and_Control_Region

Ensembl Variant Phenotype Information:

None