Variant #0000000014 (NC_000001.10:g.94522212T>G, ABCA4(NM_000350.2):c.2327A>C)

Individual ID 00000015
Chromosome 1
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.94522212T>G
Reference -
DB-ID ABCA4_000002
Average frequency (gnomAD v.2.1.1) Retrieve
Owner variome.ir
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by variome.ir
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Classification     
ABCA4 NM_000350.2 +/+ - c.2327A>C r.(?) p.(His776Pro) Likely Pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000016 DNA SEQ-NG ABCA4 1 variome.ir