Variant #0001067220 (NC_000019.9:g.46057174G>T, NC_000019.9(NM_001017989.2):c.143-24460C>A (OPA3))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.46057174G>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr19_008966
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) 2.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OPA3 NM_001017989.2 ?/. - c.143-24460C>A r.(=) p.(=)
OPA3 NM_025136.3 ?/. - c.143-5C>A r.spl? p.?


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