Variant #0000920430 (NC_000002.11:g.98999840C>G, NC_000002.11(NM_001298.2):c.396-11C>G (CNGA3))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification likely pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.98999840C>G
DNA change (hg38) g.98383377C>G
Published as -
ISCN -
DB-ID CNGA3_000116 See all 10 reported entries
Variant remarks effect on RNA predicted from in vitro mini-gene splicing assay; ACMG PP1_Supporting, PM2_Moderate, PP3_supporting, PS3_Strong
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
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 14:48:51 +01:00 (CET)
Date last edited 2023-03-02 14:49:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
CNGA3 NM_001298.2 +?/. 4i c.396-11C>G r.[(396_449del,395_396ins396-10_396-1)] p.[(Ser132_Glu150delinsArg,Ala133Phefs*13)] -


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