Variant #0004403892 (NC_000006.11:g.44270948A>G, NM_020745.3:c.2146-36delTinsC (AARS2))

Chromosome 6
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.44270948A>G
DB-ID -
dbSNP ID rs775081948
gnomAD frequency 1/245312
gnomAD homozygote count 0/122654
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     
AARS2 NM_020745.3 ./. c.2146-36delTinsC r.(=) p.(=)