Variant #0000920439 (NC_000002.11:g.99006106T>G, NC_000002.11(NM_001298.2):c.450-15T>G (CNGA3))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.99006106T>G
DNA change (hg38) g.98389643T>G
Published as -
ISCN -
DB-ID CNGA3_000259 See all 3 reported entries
Variant remarks analysis variant in in vitro mini-gene splicing assay
Reference PubMed: Reuter 2021
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2023-03-02 15:48:44 +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     

P-domain     
CNGA3 NM_001298.2 +/. 5i c.450-15T>G r.[449_450ins450-14_450-1,449_450ins[450-49_450-16;u;450-14_450-1],450_566del,=] p.[Lys151Cysfs*27,Glu150Aspfs*49,Lys151_Arg189del,=] -


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