Variant #0000127028 (NC_000001.10:g.94528251C>G, NM_000350.2:c.1819G>C (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.94528251C>G
DNA change (hg38) g.94062695C>G
Published as -
ISCN -
DB-ID ABCA4_000077 See all 17 reported entries
Variant remarks variant significantly enriched in >3000 likely Caucasian STGD1 patients compared to the non-Finnish ExAC population; another variant, giving the same predicted amino acid change, was significantly enriched in the same cohort, supporting its pathogenicity according to ACMG guidelines
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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCA4 NM_000350.2 +/. 13 c.1819G>C r.(1819g>c) p.(Gly607Arg)


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