Genomic variant #0000342773

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.193332592_193332609del
DNA change (hg38) g.193614803_193614820del
Published as OPA1:NM_130837.2:c.113_130del (Arg38_Ser43del)
ISCN -
DB-ID OPA1_000082 See all 10 reported entries
Variant remarks VKGL data sharing initiative Nederland; Variant no longer found in the VKGL dataset for this center.
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
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 ?/? 2 c.113_130del r.(?) p.(Arg38_Ser43del) -
OPA1 NM_130837.2 ?/? 2 c.113_130del r.(?) p.(Arg38_Ser43del) -