Variant #0000293414 (NC_000014.8:g.57268899T>C, NM_021728.3:c.448A>G (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.57268899T>C
DNA change (hg38) g.56802181T>C
Published as OTX2(NM_001270524.2):c.424A>G (p.I142V)
ISCN -
DB-ID OTX2_000068
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.448A>G r.(?) p.(Ile150Val)
OTX2 NM_172337.2 ?/. - c.424A>G r.(?) p.(Ile142Val)


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