Variant #0004403691 (NC_000006.11:g.44269917G>A, NM_020745.3:c.2488-10delCinsT (AARS2))

Chromosome 6
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.44269917G>A
DB-ID -
dbSNP ID rs763254942
gnomAD frequency 3/245828
gnomAD homozygote count 0/122909
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.2488-10delCinsT r.(=) p.(=)
TCTE1 NM_182539.3 ./. c.-4615C>T r.(=) p.(=)