Variant #0010001362 (NC_000016.9:g.70316628T>C, NM_001605.2:c.39A>G (AARS))

Chromosome 16
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.70316628T>C
DB-ID -
dbSNP ID rs764167027
gnomAD frequency 1/246264
gnomAD homozygote count 0/123131
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AARS NM_001605.2 ./. c.39A>G r.(?) p.(Arg13=)