Variant #0012202927 (NC_000020.10:g.34827968T>C, NM_001271874.1:c.178T>C (AAR2))

Chromosome 20
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.34827968T>C
DB-ID -
dbSNP ID rs756235658
gnomAD frequency 1/246164
gnomAD homozygote count 0/123081
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.178T>C r.(?) p.(Tyr60His)
AAR2 NM_015511.4 ./. c.178T>C r.(?) p.(Tyr60His)