Variant #0001056717 (NC_000019.9:g.46032553A>G, NM_001017989.2:c.304T>C (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.46032553A>G
DNA change (hg38) -
Published as OPA3(NM_001017989.3):c.304T>C (p.(Trp102Arg))
ISCN -
DB-ID OPA3_000036
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) 0.00011 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +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.304T>C r.(?) p.(Trp102Arg)
VASP NM_003370.3 ?/. - c.*3118A>G r.(=) p.(=)
OPA3 NM_025136.3 ?/. - c.*24219T>C r.(=) p.(=)


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