Variant #0000614417 (NC_000012.11:g.88510918T>C, NM_025114.3:c.1716A>G (CEP290))

Chromosome 12
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.88510918T>C
DNA change (hg38) g.88117141T>C
Published as CEP290(NM_025114.4):c.1716A>G (p.L572=)
ISCN -
DB-ID CEP290_000211 See all 3 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) 0.00022 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C12orf29 NM_001009894.2 -?/. - c.*68719T>C r.(=) p.(=)
CEP290 NM_025114.3 -?/. - c.1716A>G r.(?) p.(Leu572=)


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