Variant #0000000019 (NC_000017.10:g.6329101C>T, AIPL1(NM_014336.3):c.834G>A)

Individual ID 00000021
Chromosome 17
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.6329101C>T
Reference -
DB-ID AIPL1_000001
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Classification     
AIPL1 NM_014336.3 +/+ - c.834G>A r.(?) p.(Trp278*) Pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000022 DNA SEQ-NG AIPL1 1 variome.ir