Variant #0006099880 (NC_000009.11:g.99413775A>G, NM_153698.1:c.318T>C (AAED1))

Chromosome 9
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.99413775A>G
DB-ID -
dbSNP ID rs769796460
gnomAD frequency 1/239424
gnomAD homozygote count 0/119711
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.318T>C r.(?) p.(Pro106=)