View genomic variant #0000016293

Chromosome 10
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.101473218A>G
Published as -
GERP -
Segregation -
DB-ID COX15_000013
MSCV MSCV_0016293
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.83485 View details
Owner LOVD




Variant on transcripts

3 entries on 1 page. Showing entries 1 - 3.
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Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
COX15 00000083 NM_004376.5 0000016293 ./. - - c.1120T>C p.(Phe374Leu) - - - -
COX15 00000084 NM_078470.4 0000016293 ./. - - c.*1126T>C p.(=) - - - -
COX15 00000082 XM_005269539.1 0000016293 ./. - - c.1101+2887T>C p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000116814; RCV000259999; RCV000676871;
Chromosome 10:101473218..101473218
Allele frequencies from ESP 0.83485
Allele frequencies from ExAC 0.86101
Allele frequencies from TGP 0.82708
ClinVar Allele ID 134284
Disease database name and identifier MedGen:CN169374|MedGen:C3661900|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name not specified|not provided|Leigh syndrome
HGVS variant names NC 000010.10:g.101473218A>G
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA288774
Gene symbol:Gene id. COX15:1355
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant, SO:0001624|3 prime UTR variant, SO:0001627|intron variant
Allele origin germline
dbSNP ID 2231687
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None