Genomic variant #0000406295

Individual ID 00181458
Chromosome 3
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.193332512T>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID OPA1_000464
Variant remarks -
Reference PubMed: Chen 2014
ClinVar ID -
dbSNP ID -
Origin Germline/De novo (untested)
Segregation -
Frequency -
Re-site Hpy188I+, BtsIMutI-, TspRI-
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Thomas Foulonneau




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

P-domain     
OPA1 NM_015560.2 +/+? - c.33T>A - r.(?) p.(Cys11*) -
OPA1 NM_130837.2 +/+? - c.33T>A pathogenic r.(?) p.(Cys11*) -



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000182419 DNA SEQ Blood - OPA1 1 Thomas Foulonneau