Variant #0000293374 (NC_000019.9:g.46032338T>A, NM_001017989.2:c.519A>T (OPA3))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.46032338T>A
DNA change (hg38) g.45529080T>A
Published as OPA3(NM_001017989.3):c.519A>T (p.P173=)
ISCN -
DB-ID OPA3_000005
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) 0.00016 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OPA3 NM_001017989.2 -/. - c.519A>T r.(?) p.(Pro173=)
VASP NM_003370.3 -/. - c.*2903T>A r.(=) p.(=)
OPA3 NM_025136.3 -/. - c.*24434A>T r.(=) p.(=)


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