Variant #0010590377 (NC_000017.10:g.41116455C>T, NM_001261434.1:c.3G>A (AARSD1))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.41116455C>T
DB-ID -
dbSNP ID rs776665995
gnomAD frequency 2/142048
gnomAD homozygote count 0/71022
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.*4710G>A r.(=) p.(=)
PTGES3L NM_001142654.1 ./. c.*4710G>A r.(=) p.(=)
PTGES3L NM_001261430.1 ./. c.*4710G>A r.(=) p.(=)
AARSD1 NM_001261434.1 ./. c.3G>A r.(?) p.(Met1?)