View genomic variant #0000004949

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.8932C>T
Published as -
GERP 0.456
Segregation -
DB-ID chrM_001216 See all 2 reported entries
MSCV MSCV_0004949
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 0000004949 +?/+? - . c.406C>T p.P136S - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000224223; RCV000854366; RCV001526415;
Chromosome M:8932..8932
ClinVar Allele ID 237030
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0044970, MeSH:D028361, MedGen:C0751651, Orphanet:68380|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name not provided|Mitochondrial disease|Leigh syndrome
HGVS variant names NC 012920.1:m.8932C>T
ClinVar review status reviewed by expert panel
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA10581280
Gene symbol:Gene id. MT-ATP6:4508
Allele origin germline
dbSNP ID 878853013
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-ATP6Prostate CancerC8932TP-S+-ReportedCoding_and_Control_Region

Ensembl Variant Phenotype Information:

None