Variant #0000549338 (NC_000012.11:g.88472996C>T, NM_025114.3:c.5237G>A (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.88472996C>T
DNA change (hg38) g.88079219C>T
Published as CEP290(NM_025114.3):c.5237G>A (p.(Arg1746Gln)), CEP290(NM_025114.4):c.5237G>A (p.R1746Q)
ISCN -
DB-ID CEP290_000189 See all 10 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) 0.01067 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C12orf29 NM_001009894.2 -?/. - c.*30797C>T r.(=) p.(=)
CEP290 NM_025114.3 -?/. - c.5237G>A r.(?) p.(Arg1746Gln)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.