Variant #0000127187 (NC_000001.10:g.(94506959_94508316)_(94510301_94512474)del, NC_000001.10(NM_000350.2):c.(2918+1_2919-1)_(3328+1_3329-1)del (ABCA4))

Chromosome 1
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.(94506959_94508316)_(94510301_94512474)del
DNA change (hg38) g.(94041403_94042760)_(94044745_94046918)del
Published as c.2919-?_3328+?del
ISCN -
DB-ID ABCA4_000041 See all 26 reported entries
Variant remarks -
Reference PubMed: Cornelis 2017, Journal: Cornelis 2017, Journal: Cornelis 2023
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Stéphanie Cornelis
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Stéphanie Cornelis
Date created 2016-07-29 12:46:24 +02:00 (CEST)
Date last edited 2024-09-25 14:18:42 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCA4 NM_000350.2 +/. 19i_22i c.(2918+1_2919-1)_(3328+1_3329-1)del r.(2919_3328del) p.?


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.