View genomic variant #0000004065

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.14680C>A
Published as -
GERP -3.110
Segregation -
DB-ID chrM_000440
MSCV MSCV_0004065
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-TE 00001349 MT-TE-201 0000004065 +?/+? - . . . - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV002248003;
Chromosome M:14680..14680
ClinVar Allele ID 1676936
Disease database name and identifier MedGen:CN169374
ClinVar preferred disease name not specified
HGVS variant names NC 012920.1:m.14680C>A
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. MT-TE:4556
Allele origin germline
dbSNP ID 2124598415
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-TEMitochondrial encephalomyopathyC14680AtRNA Glu-+ReportedRNA

Ensembl Variant Phenotype Information:

None