Variant #0000273643 (NC_000004.11:g.47944132C>T, NM_001142564.1:c.690G>A (CNGA1))

Chromosome 4
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.47944132C>T
DNA change (hg38) g.47942115C>T
Published as CNGA1(NM_001142564.1):c.690G>A (p.S230=)
ISCN -
DB-ID CNGA1_000013
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-16 12:55:17 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CNGA1 NM_000087.3 ?/. - c.483G>A r.(?) p.(Ser161=)
CNGA1 NM_001142564.1 ?/. - c.690G>A r.(?) p.(Ser230=)


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