Variant #0010001363 (NC_000016.9:g.70316629C>T, NM_001605.2:c.38G>A (AARS))

Chromosome 16
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.70316629C>T
DB-ID -
dbSNP ID rs774437336
gnomAD frequency 1/246262
gnomAD homozygote count 0/123130
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     
AARS NM_001605.2 ./. c.38G>A r.(?) p.(Arg13Gln)