Screening #0000182460

Individual ID 00181499
Template DNA
Technique SEQ-NG
Tissue Muscle, peripheral blood, lymphocytes, fibroblasts
Remarks -
Variants found? 1
Owner name Thomas FOULONNEAU


Genes screened


AscendingSymbol     

Gene     

Chr     

Band

Transcripts     

Variants     

Unique variants     

Last updated     

Associated with diseases
OPA1 optic atrophy 1 (autosomal dominant) 3 q28-q29 2 769 525 2019-06-14 BEHRS, MTDPS-14, OPA, OPA+, OPA-1, glaucoma, normal tension, susceptibility to



Variants found

1 entry on 1 page. Showing entry 1.
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Chr     

Allele     

AscendingDNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     

Gene     

Effect     

Codon change     

IDbase Accession Number     

VariO/DNA     

VariO/Protein     

VariO/RNA     

Exon     

DNA change (cDNA)     

Haplotype     

ClassClinical     

RNA change     

Protein     

P-domain     

Exon_old     

DNA/Legacy     

Function/GVS     

Protein/Legacy     

CodonNr     

Method     

Predict/AGVGD     

Predict/Grantham     

Predict/MutationTaster     

Predict/PolyPhen     

Predict/PolyPhenScore     

Predict/SIFT     

Predicted     

Type/DNA     

Conservation     

CpG     

Enzyme activity     

mRNA level     

Predict/CADD     

Predict/Splice     

Protein/Stain     

Protein level     
3 Parent #1 g.193332669_193332673del - - - OPA1_000459 - PubMed: Nasca 2017 - - Germline/De novo (untested) - - EarI-,MboII- 0 - Thomas FOULONNEAU OPA1 -/-? - - - - - - NM_015560.2:c.190_194del, NM_130837.2:c.190_194del - , benign r.(?) p.(Ser64Aspfs*7) - - - - - - - - - - - - - - - - - - - - - - -
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