Variant #0000518775 (NC_000003.11:g.193311159C>T, OPA1(NM_015560.2):c.-8C>T)

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.193311159C>T
DNA change (hg38) g.193593370C>T
Published as -
ISCN -
DB-ID OPA1_000545
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (large NGS studies) 0.00012 View details
Owner VKGL-NL_Nijmegen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
OPA1 NM_015560.2 ?/. - c.-8C>T r.(?) p.(=) -
OPA1 NM_130837.2 ?/. - c.-8C>T r.(?) p.(=) -