Variant #0000817952 (NC_000016.9:g.57984428_57984449dup, NC_000016.9(NM_001297.4):c.875-5_891dup (CNGB1))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.57984428_57984449dup
DNA change (hg38) g.57950524_57950545dup
Published as -
ISCN -
DB-ID CNGB1_000192 See all 3 reported entries
Variant remarks -
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 2021-11-03 08:58:41 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CNGB1 NM_001297.4 +?/. 12i_13 c.875-5_891dup r.spl p.?


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