Variant #0012202919 (NC_000020.10:g.34827932G>T, NM_001271874.1:c.142G>T (AAR2))

Chromosome 20
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.34827932G>T
DB-ID -
dbSNP ID rs111591742
gnomAD frequency 1061/246216
gnomAD homozygote count 12/122054
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     
AAR2 NM_001271874.1 ./. c.142G>T r.(?) p.(Val48Leu)
AAR2 NM_015511.4 ./. c.142G>T r.(?) p.(Val48Leu)