Variant #0000816586 (NC_000016.9:g.57994384A>G, NC_000016.9(NM_001297.4):c.583+2T>C (CNGB1))

Chromosome 16
Allele Parent #1
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.57994384A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID CNGB1_000246 See all 3 reported entries
Variant remarks in vitro splicing assay shows exon skipping
Reference PubMed: Mauro-Herrera 2021
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 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 2021-10-26 19:48:03 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CNGB1 NM_001297.4 +/. - c.583+2T>C r.(535_583del) p.(Val179Argfs*82)


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