Variant #0000609216 (NC_000004.11:g.47951884del, NM_001142564.1:c.472del (CNGA1))

Chromosome 4
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.47951884del
DNA change (hg38) g.47949867del
Published as CNGA1(NM_001142564.1):c.472delC (p.L158Ffs*4)
ISCN -
DB-ID CNGA1_000047 See all 16 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) 0.0001 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 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-06-16 12:55:21 +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.265del r.(?) p.(Leu89PhefsTer4)
CNGA1 NM_001142564.1 +/. - c.472del r.(?) p.(Leu158PhefsTer4)


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