Variant #0000539511 (NC_000010.10:g.13154576C>T, NM_001008211.1:c.493C>T (OPTN))

Chromosome 10
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.13154576C>T
DNA change (hg38) g.13112576C>T
Published as OPTN(NM_001008211.1):c.493C>T (p.Q165*), OPTN(NM_001008212.2):c.493C>T (p.(Gln165Ter))
ISCN -
DB-ID OPTN_000019 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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OPTN NM_001008211.1 +/. - c.493C>T r.(?) p.(Gln165Ter)


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