Variant #0004404814 (NC_000006.11:g.44280770C>G, NC_000006.11(NM_020745.3):c.243+48G>C (AARS2))

Chromosome 6
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.44280770C>G
DB-ID -
dbSNP ID rs768951009
gnomAD frequency 1/235920
gnomAD homozygote count 0/117959
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     
AARS2 NM_020745.3 ./. c.243+48G>C r.(=) p.(=)