Variant #0000957955 (NC_000012.11:g.88532970T>A, NC_000012.11(NM_025114.3):c.251-2A>T (CEP290))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.88532970T>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID CEP290_000627
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-01-24 20:25:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CEP290 NM_025114.3 +?/. - c.251-2A>T r.(?) p.(?)


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