Variant #0000817945 (NC_000016.9:g.57994761dup, NM_001297.4:c.522dup (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.57994761dup
DNA change (hg38) g.57960857dup
Published as -
ISCN -
DB-ID CNGB1_000284 See all 5 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 +/. 8 c.522dup r.(?) p.(Lys175Glnfs*4)


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