Variant #0000522620 (NC_000004.11:g.47954625G>A, NM_001142564.1:c.301C>T (CNGA1))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.47954625G>A
DNA change (hg38) g.47952608G>A
Published as CNGA1(NM_000087.3):c.94C>T (p.(Arg32Ter)), CNGA1(NM_001142564.2):c.82C>T (p.R28*)
ISCN -
DB-ID CNGA1_000026 See all 19 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) 8.0E-5 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     
CNGA1 NM_000087.3 +?/. - c.94C>T r.(?) p.(Arg32Ter)
CNGA1 NM_001142564.1 +?/. - c.301C>T r.(?) p.(Arg101Ter)


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