Variant #0001013969 (NC_000004.11:g.47939552G>A, NM_001142564.1:c.1166C>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.47939552G>A
DNA change (hg38) -
Published as CNGA1(NM_000087.5):c.947C>T (p.S316F), CNGA1(NM_001142564.1):c.1166C>T (p.S389F), CNGA1(NM_001142564.2):c.947C>T (p.S316F)
ISCN -
DB-ID CNGA1_000011 See all 21 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) 0.00107 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CNGA1 NM_000087.3 +?/. - c.959C>T r.(?) p.(Ser320Phe)
CNGA1 NM_001142564.1 +?/. - c.1166C>T r.(?) p.(Ser389Phe)


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