Variant #0010590043 (NC_000017.10:g.41108310G>C, NM_025267.3:c.913delCinsG (PTGES3L-AARSD1))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.41108310G>C
DB-ID -
dbSNP ID -
gnomAD frequency 1/246260
gnomAD homozygote count 0/123128
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.1096delCinsG r.(?) p.(His366Asp)
AARSD1 NM_001261434.1 ./. c.574delCinsG r.(?) p.(His192Asp)
PTGES3L-AARSD1 NM_025267.3 ./. c.913delCinsG r.(?) p.(His305Asp)