Variant #0000518779 (NC_000003.11:g.193332567C>T, OPA1(NM_015560.2):c.88C>T)

Chromosome 3
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.193332567C>T
DNA change (hg38) g.193614778C>T
Published as OPA1(NM_130837.3):c.88C>T (p.L30=)
ISCN -
DB-ID OPA1_000548
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
OPA1 NM_015560.2 -?/. - c.88C>T r.(?) p.(Leu30=) -
OPA1 NM_130837.2 -?/. - c.88C>T r.(?) p.(Leu30=) -