Variant #0000808943 (NC_000019.9:g.46032414del, NM_001017989.2:c.445del (OPA3))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.46032414del
DNA change (hg38) -
Published as OPA3(NM_001017989.2):c.445delC (p.L149Wfs*67), OPA3(NM_001017989.3):c.445delC (p.L149Wfs*67)
ISCN -
DB-ID OPA3_000011 See all 3 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OPA3 NM_001017989.2 +/. - c.445del r.(?) p.(Leu149TrpfsTer67)
VASP NM_003370.3 +/. - c.*2979del r.(?) p.(=)
OPA3 NM_025136.3 +/. - c.*24360del r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.