Variant #0006099933 (NC_000009.11:g.99414041T>A, NC_000009.11(NM_153698.1):c.262-47A>T (AAED1))

Chromosome 9
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.99414041T>A
DB-ID -
dbSNP ID rs372440123
gnomAD frequency 2/226046
gnomAD homozygote count 0/112597
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AAED1 NM_153698.1 ./. c.262-47A>T r.(=) p.(=)