Variant #0000863777 (NC_000015.9:g.28326863del, NM_000275.2:c.163del (OCA2))

Chromosome 15
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.28326863del
DNA change (hg38) -
Published as OCA2(NM_000275.2):c.163delG (p.(Ala55Leufs*47)), OCA2(NM_000275.2):c.163delG (p.A55Lfs*47), OCA2(NM_000275.3):c.163delG (p.A55Lfs*47)
ISCN -
DB-ID OCA2_000026 See all 5 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) 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 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OCA2 NM_000275.2 +/. - c.163del r.(?) p.(Ala55LeufsTer47)


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