Variant #0010590459 (NC_000017.10:g.41121212_41121213insA, NM_001261434.1:c.-4756_-4755insT (AARSD1))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.41121212_41121213insA
DB-ID -
dbSNP ID rs771367214
gnomAD frequency 1/3578
gnomAD homozygote count 0/113
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.463-10_463-9insT r.(=) p.(=)
PTGES3L NM_001142654.1 ./. c.448-10_448-9insT r.(=) p.(=)
PTGES3L NM_001261430.1 ./. c.562-10_562-9insT r.(=) p.(=)
AARSD1 NM_001261434.1 ./. c.-4756_-4755insT r.(=) p.(=)