Variant #0006099963 (NC_000009.11:g.99417334T>G, NC_000009.11(NM_153698.1):c.192+38A>C (AAED1))

Chromosome 9
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.99417334T>G
DB-ID -
dbSNP ID rs771491568
gnomAD frequency 1/69068
gnomAD homozygote count 0/34533
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.192+38A>C r.(=) p.(=)