Variant #0000549426 (NC_000012.11:g.88533296C>T, NM_025114.3:c.226G>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.88533296C>T
DNA change (hg38) g.88139519C>T
Published as CEP290(NM_025114.3):c.226G>A (p.A76T, p.(Ala76Thr)), CEP290(NM_025114.4):c.226G>A (p.A76T)
ISCN -
DB-ID CEP290_000276 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) 0.00062 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-11-27 17:27:23 +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.*91097C>T r.(=) p.(=)
CEP290 NM_025114.3 ?/. - c.226G>A r.(?) p.(Ala76Thr)
TMTC3 NM_181783.3 ?/. - c.-2997C>T r.(?) p.(=)


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