Variant #0000920420 (NC_000002.11:g.98986540G>A, NC_000002.11(NM_001298.2):c.101+1G>A (CNGA3))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.98986540G>A
DNA change (hg38) g.98370077G>A
Published as -
ISCN -
DB-ID CNGA3_000080 See all 10 reported entries
Variant remarks effect on RNA predicted from in vitro mini-gene splicing assay; ACMG PS1_Very strong, PM2_Moderate, PP5_Supporting, PP3_supporting, PS3_Strong
Reference -
ClinVar ID VCV000208567
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00027 View details
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 14:09:00 +01:00 (CET)
Date last edited 2023-03-02 14:21:39 +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 +/. 2i c.101+1G>A r.(52_101del) p.(Val18Serfs*6) -


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