Variant #0000719311 (NC_000003.11:g.193332717T>C, NM_015560.2:c.238T>C (OPA1))

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.193332717T>C
DNA change (hg38) -
Published as OPA1(NM_130837.2):c.238T>C (p.Y80H)
ISCN -
DB-ID OPA1_000598
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
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.238T>C r.(?) p.(Tyr80His) -
OPA1 NM_130837.2 -?/. - c.238T>C r.(?) p.(Tyr80His) -


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