Variant #0000818010 (NC_000016.9:g.57935275T>A, NM_001297.4:c.2957A>T (CNGB1))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification likely pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.57935275T>A
DNA change (hg38) g.57901371T>A
Published as -
ISCN -
DB-ID CNGB1_000004 See all 72 reported entries
Variant remarks ACMG PM1, PM2, PP3, PP5
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00119 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 2021-10-31 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 +?/. 29 c.2957A>T r.(?) p.(Asn986Ile)


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