Variant #0000890812 (NC_000012.11:g.88443080A>T, NM_025114.3:c.7321T>A (CEP290))

Chromosome 12
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.88443080A>T
DNA change (hg38) -
Published as CEP290(NM_025114.4):c.7321T>A (p.L2441I)
ISCN -
DB-ID CEP290_000601
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C12orf29 NM_001009894.2 ?/. - c.*881A>T r.(=) p.(=)
CEP290 NM_025114.3 ?/. - c.7321T>A r.(?) p.(Leu2441Ile)


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