View genomic variant #0000016276

Chromosome 10
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.101471854A>G
Published as -
GERP -
Segregation -
DB-ID COX15_000034
MSCV MSCV_0016276
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

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

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 0000016276 ./. - - c.*1317T>C p.(=) - - - -
COX15 00000084 NM_078470.4 0000016276 ./. - - c.*2490T>C p.(=) - - - -
COX15 00000082 XM_005269539.1 0000016276 ./. - - c.1101+4251T>C p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000294256;
Chromosome 10:101471854..101471854
ClinVar Allele ID 311939
Disease database name and identifier MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:ORPHA506, SNOMED CT:29570005
ClinVar preferred disease name Leigh syndrome
HGVS variant names NC 000010.10:g.101471854A>G
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported Illumina Clinical Services Laboratory, Illumina:774465
Gene symbol:Gene id. COX15:1355
Molecular consequence SO:0001619|non-coding transcript variant, SO:0001624|3 prime UTR variant, SO:0001627|intron variant
Allele origin germline
dbSNP ID 886046604
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