Variant #0000816587 (NC_000016.9:g.57946932C>T, NC_000016.9(NM_001297.4):c.2305-34G>A (CNGB1))

Chromosome 16
Allele Parent #2
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.57946932C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID CNGB1_000247 See all 3 reported entries
Variant remarks minigene 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) 8.0E-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 19:54:28 +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.2305-34G>A r.[(2218_2369del,2305_2369del,2218_2304del)] p.(?)


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