Variant #0000552707 (NC_000014.8:g.57268652_57268662del, NM_021728.3:c.686_696del (OTX2))

Chromosome 14
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.57268652_57268662del
DNA change (hg38) g.56801934_56801944del
Published as OTX2(NM_021728.3):c.686_696del (p.(Pro229GlnfsTer27))
ISCN -
DB-ID OTX2_000078
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +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.686_696del r.(?) p.(Pro229GlnfsTer27)
OTX2 NM_172337.2 +?/. - c.662_672del r.(?) p.(Pro221GlnfsTer27)


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