Variant #0001026393 (NC_000014.8:g.57272114C>G, NM_021728.3:c.61G>C (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.57272114C>G
DNA change (hg38) -
Published as OTX2(NM_021728.4):c.61G>C (p.G21R)
ISCN -
DB-ID OTX2_000132
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OTX2 NM_021728.3 ?/. - c.61G>C r.(?) p.(Gly21Arg)
OTX2 NM_172337.2 ?/. - c.61G>C r.(?) p.(Gly21Arg)


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