Variant #0003481623 (NC_000004.11:g.171010833G>A, NM_016228.3:c.9C>T (AADAT))

Chromosome 4
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.171010833G>A
DB-ID -
dbSNP ID -
gnomAD frequency 1/246168
gnomAD homozygote count 0/123083
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     
AADAT NM_016228.3 ./. c.9C>T r.(?) p.(Tyr3=)
AADAT NM_182662.1 ./. c.9C>T r.(?) p.(Tyr3=)