Variant #0010782244 (NC_000017.10:g.66985983G>A, NM_080283.3:c.3926delCinsT (ABCA9))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.66985983G>A
DB-ID -
dbSNP ID rs145276039
gnomAD frequency 94/245272
gnomAD homozygote count 1/122542
Average frequency (gnomAD v.2.1.1) Retrieve
Database submission license No license selected
Created by LOVD
Date created 2017-02-27 00:00:00 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCA9 NM_080283.3 ./. c.3926delCinsT r.(?) p.(Thr1309Ile)