Variant #0000817940 (NC_000016.9:g.57998062G>A, NM_001297.4:c.262C>T (CNGB1))

Chromosome 16
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.57998062G>A
DNA change (hg38) g.57964158G>A
Published as -
ISCN -
DB-ID CNGB1_000002 See all 7 reported entries
Variant remarks ACMG PVS1, PM2, PP1, PP3
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 2021-10-31 14:57:51 +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     
CNGB1 NM_001297.4 +/. 4 c.262C>T r.(?) p.(Gln88*)


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