Variant #0000808945 (NC_000019.9:g.46032673C>T, NM_001017989.2:c.184G>A (OPA3))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.46032673C>T
DNA change (hg38) -
Published as OPA3(NM_001017989.2):c.184G>A (p.G62S), OPA3(NM_001017989.3):c.184G>A (p.G62S)
ISCN -
DB-ID OPA3_000006 See all 2 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) 0.00054 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 2021-09-17 14:40:49 +02:00 (CEST)
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.184G>A r.(?) p.(Gly62Ser)
VASP NM_003370.3 -?/. - c.*3238C>T r.(=) p.(=)
OPA3 NM_025136.3 -?/. - c.*24099G>A r.(=) p.(=)


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