Variant #0000853844 (NC_000014.8:g.57271037G>T, NM_021728.3:c.142C>A (OTX2))

Chromosome 14
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.57271037G>T
DNA change (hg38) -
Published as OTX2(NM_001270524.1):c.118C>A (p.R40=)
ISCN -
DB-ID OTX2_000124
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 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OTX2 NM_021728.3 -?/. - c.142C>A r.(?) p.(Arg48=)
OTX2 NM_172337.2 -?/. - c.118C>A r.(?) p.(Arg40=)


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