Variant #0006099940 (NC_000009.11:g.99416960C>T, NC_000009.11(NM_153698.1):c.261+27G>A (AAED1))

Chromosome 9
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.99416960C>T
DB-ID -
dbSNP ID rs73543002
gnomAD frequency 862/150822
gnomAD homozygote count 44/74593
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     
AAED1 NM_153698.1 ./. c.261+27G>A r.(=) p.(=)