Variant #0000304892 (NC_000014.8:g.57268604G>A, NM_021728.3:c.743C>T (OTX2))

Chromosome 14
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.57268604G>A
DNA change (hg38) g.56801886G>A
Published as OTX2(NM_001270524.1):c.719C>T (p.T240I), OTX2(NM_021728.4):c.743C>T (p.(Thr248Ile))
ISCN -
DB-ID OTX2_000065 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) 6.0E-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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OTX2 NM_021728.3 ?/. - c.743C>T r.(?) p.(Thr248Ile)
OTX2 NM_172337.2 ?/. - c.719C>T r.(?) p.(Thr240Ile)


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