Variant #0009999931 (NC_000016.9:g.70286602T>C, NM_001605.2:c.*22delAinsG (AARS))

Chromosome 16
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.70286602T>C
DB-ID -
dbSNP ID rs776068061
gnomAD frequency 4/245944
gnomAD homozygote count 0/122967
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.*22delAinsG r.(=) p.(=)
EXOSC6 NM_058219.2 ./. c.-799A>G r.(=) p.(=)