Variant #0000518782 (NC_000003.11:g.193332724A>G, OPA1(NM_015560.2):c.245A>G)

Chromosome 3
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.193332724A>G
DNA change (hg38) g.193614935A>G
Published as OPA1(NM_130837.3):c.245A>G (p.Y82C)
ISCN -
DB-ID OPA1_000468 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) 2.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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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.245A>G r.(?) p.(Tyr82Cys) -
OPA1 NM_130837.2 ?/. - c.245A>G r.(?) p.(Tyr82Cys) -