Variant #0000805967 (NC_000012.11:g.88514835T>C, NM_025114.3:c.1298A>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.88514835T>C
DNA change (hg38) -
Published as CEP290(NM_025114.3):c.1298A>G (p.D433G), CEP290(NM_025114.4):c.1298A>G (p.D433G)
ISCN -
DB-ID CEP290_000224 See all 8 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) 0.00132 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-09-17 14:40:49 +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     
C12orf29 NM_001009894.2 -?/. - c.*72636T>C r.(=) p.(=)
CEP290 NM_025114.3 -?/. - c.1298A>G r.(?) p.(Asp433Gly)


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