Variant #0000689304 (NC_000004.11:g.47954680C>T, NM_001142564.1:c.246G>A (CNGA1))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.47954680C>T
DNA change (hg38) -
Published as CNGA1(NM_001142564.1):c.246G>A (p.Q82=), CNGA1(NM_001142564.2):c.27G>A (p.Q9=)
ISCN -
DB-ID CNGA1_000071 See all 2 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 2020-09-15 15:50:26 +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.39G>A r.(?) p.(Gln13=)
CNGA1 NM_001142564.1 -?/. - c.246G>A r.(?) p.(Gln82=)


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