Variant #0004404861 (NC_000006.11:g.44281018C>T, NM_020745.3:c.43G>A (AARS2))

Chromosome 6
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.44281018C>T
DB-ID -
dbSNP ID -
gnomAD frequency 5/209080
gnomAD homozygote count 0/104535
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     
AARS2 NM_020745.3 ./. c.43G>A r.(?) p.(Ala15Thr)