Variant #0000616060 (NC_000016.9:g.57938771C>A, NM_001297.4:c.2501G>T (CNGB1))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.57938771C>A
DNA change (hg38) g.57904867C>A
Published as CNGB1(NM_001297.4):c.2501G>T (p.R834L), CNGB1(NM_001297.5):c.2501G>T (p.R834L)
ISCN -
DB-ID CNGB1_000049 See all 4 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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CNGB1 NM_001297.4 ?/. - c.2501G>T r.(?) p.(Arg834Leu)


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