Variant #0000246249 (NC_000004.11:g.47944120A>G, NM_001142564.1:c.702T>C (CNGA1))

Chromosome 4
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.47944120A>G
DNA change (hg38) g.47942103A>G
Published as CNGA1(NM_001142564.2):c.483T>C (p.Y161=)
ISCN -
DB-ID CNGA1_000023
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) 0.00095 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 2018-01-15 20:58:59 +01:00 (CET)
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.495T>C r.(?) p.(Tyr165=)
CNGA1 NM_001142564.1 -/. - c.702T>C r.(?) p.(Tyr234=)


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