Full data view for gene OPA1

Mitodyn.org logo
A database from the MITOchondrial DYNamics variation portal "Mitodyn.org".
This database is also one of the "Eye disease" gene variant databases.
 
Information The variants shown are described using the transcript reference sequence.

9 entries on 1 page. Showing entries 1 - 9.
Legend   How to query  

Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

Classification method     

Clinical classification     

DNA 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     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
?/. 2 c.113_130del r.(?) p.(Arg38_Ser43del) - Unknown - VUS g.193332592_193332609del g.193614803_193614820del - - OPA1_000082 - - - - Germline - - - 0 - DNA SEQ-NG - - SPG18 - - - - - - - - 0 - - 1 Erik-Jan Kamsteeg
./. - c.113_130del r.(?) p.(Arg38_Ser43del) - Unknown - pathogenic g.193332592_193332609del g.193614803_193614820del 112_139del18 - OPA1_000082 eOPA1 identifier (obsolete):OA_00091; Nucleotide change: Deletion of 18 nucleotides at 112_129 (reference: OPA1 transcript variant 1, NM_015560.1); Note: This mutation name has been modified according to the Nomenclature Working Group nomenclature PubMed: Thiselton 2002 - - Germline - - - 0 - DNA SEQ Blood - OPA - PubMed: Thiselton 2002 - - - Denmark - - 0 - - 1 Marc Ferre
./. - c.113_130del r.(?) p.(Arg38_Ser43del) - Unknown - pathogenic g.193332592_193332609del g.193614803_193614820del 112_139del18 - OPA1_000082 eOPA1 identifier (obsolete):OA_00091; Nucleotide change: Deletion of 18 nucleotides at 112_129 (reference: OPA1 transcript variant 1, NM_015560.1); Note: This mutation name has been modified according to the Nomenclature Working Group nomenclature PubMed: Thiselton 2002 - - Germline - - - 0 - DNA SEQ Blood - OPA - - - M - France - - 0 - - 1 Angelique Caignard
./. - c.113_130del r.(?) p.(Arg38_Ser43del) - Parent #1 - likely pathogenic g.193332592_193332609del g.193614803_193614820del - - OPA1_000082 - Mavrogiannis LA, Charlton RS (unpublished) - - Germline - - - 0 - DNA SEQ - - OPA - Mavrogiannis LA, Charlton RS (unpublished) - - - - - - 0 - - 1 Lampros Mavrogiannis
./. - c.113_130del r.(?) p.(Arg38_Ser43del) - Unknown - pathogenic g.193332592_193332609del g.193614803_193614820del - - OPA1_000082 - - - - Germline - - - 0 - DNA SEQ - - OPA - - - F - United States European - 0 - - 1 Bjorn Oskarsson
-/. 2 c.113_130del r.(?) p.(Arg38_Ser43del) - Maternal (confirmed) - benign g.193332592_193332609del g.193614803_193614820del 113_130del18 - OPA1_000082 - PubMed: Tingaud-Sequeira 2017 - rs761926672 Germline - - - 0 - DNA SEQ - - PHARC 27890673-FamPatII1 PubMed: Tingaud-Sequeira 2017 3-generation family, 1 affected, unaffected heterozygous carrier parents F no Sweden - - 0 - - 1 Johan den Dunnen
?/. 2 c.113_130del r.(?) p.(Arg38_Ser43del) - Unknown - VUS g.193332592_193332609del g.193614803_193614820del - - OPA1_000082 - Le Roux 2019, submitted - - Germline - - - 0 - DNA SEQ Blood - OPA - Le Roux 2019, submitted Updated from Lab-ID: ANG2013#8 M - France - - 0 - - 1 Bastien Le Roux
+/+? - c.113_130del r.(?) p.(Arg38_Ser43del) - Parent #1 - pathogenic g.193332592_193332609del g.193614803_193614820del - - OPA1_000082 - Amati-Bonneau P, Angers 2012 (unpublished); Le Roux 2019, submitted - - Germline/De novo (untested) - - Hpy188III- 0 - DNA SEQ Blood - OPA - Amati-Bonneau P, Angers 2012 (unpublished); Le Roux 2019, submitted - - - (France) - - 0 - - 1 Marc Ferre
-?/. - c.113_130del r.(?) p.(Arg38_Ser43del) - Unknown - likely benign g.193332592_193332609del g.193614803_193614820del OPA1(NM_130837.2):c.113_130delGAAGCATTTATCATTCAC (p.R38_S43del) - OPA1_000082 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
Legend   How to query