Variant #0010590069 (NC_000017.10:g.41108398C>T, NM_025267.3:c.885+23delGinsA (PTGES3L-AARSD1))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.41108398C>T
DB-ID -
dbSNP ID rs749367409
gnomAD frequency 3/246022
gnomAD homozygote count 0/123005
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-AARSD1 NM_001136042.2 ./. c.1068+23delGinsA r.(=) p.(=)
AARSD1 NM_001261434.1 ./. c.546+23delGinsA r.(=) p.(=)
PTGES3L-AARSD1 NM_025267.3 ./. c.885+23delGinsA r.(=) p.(=)