Variant #0010590442 (NC_000017.10:g.41121206_41121209del, NM_001261434.1:c.-4752_-4749del (AARSD1))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.41121206_41121209del
DB-ID -
dbSNP ID rs868786464
gnomAD frequency 2/50696
gnomAD homozygote count 0/3022
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     
PTGES3L NM_001142653.1 ./. c.463-6_463-3del r.spl? p.?
PTGES3L NM_001142654.1 ./. c.448-6_448-3del r.spl? p.?
PTGES3L NM_001261430.1 ./. c.562-6_562-3del r.spl? p.?
AARSD1 NM_001261434.1 ./. c.-4752_-4749del r.(=) p.(=)