Variant #0000928752 (NC_000003.11:g.193363569del, NM_015560.2:c.1569del (OPA1))

Chromosome 3
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.193363569del
DNA change (hg38) -
Published as OPA1(NM_130837.3):c.1734delT (p.Q579Rfs*6)
ISCN -
DB-ID OPA1_000499 See all 4 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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
OPA1 NM_015560.2 +/. - c.1569del r.(?) p.(Gln524Argfs*6) -
OPA1 NM_130837.2 +/. - c.1734del r.(?) p.(Gln579Argfs*6) -


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