Variant #0010590448 (NC_000017.10:g.41121207G>A, NM_001261434.1:c.-4750C>T (AARSD1))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.41121207G>A
DB-ID -
dbSNP ID rs533186249
gnomAD frequency 59/103372
gnomAD homozygote count 2/3045
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     
PTGES3L NM_001142653.1 ./. c.463-4delCinsT r.spl? p.?
PTGES3L NM_001142654.1 ./. c.448-4delCinsT r.spl? p.?
PTGES3L NM_001261430.1 ./. c.562-4delCinsT r.spl? p.?
AARSD1 NM_001261434.1 ./. c.-4750C>T r.(=) p.(=)