Variant #0000535383 (NC_000008.10:g.87656009del, NM_019098.4:c.1148del (CNGB3))

Chromosome 8
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.87656009del
DNA change (hg38) g.86643781del
Published as CNGB3(NM_019098.4):c.1148delC (p.(Thr383Ilefs*13)), CNGB3(NM_019098.4):c.1148delC (p.T383Ifs*13), CNGB3(NM_019098.5):c.1148delC (p.T383Ifs*13)
ISCN -
DB-ID CNGB3_000001 See all 452 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00174 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CNGB3 NM_019098.4 +/. - c.1148del r.(?) p.(Thr383IlefsTer13)


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