Variant #0000623680 (NC_000017.10:g.41108574C>T, PTGES3L-AARSD1(NM_025267.3):c.732G>A)

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.41108574C>T
DNA change (hg38) g.42956557C>T
Published as AARSD1(NM_001261434.2):c.393G>A (p.E131=), PTGES3L-AARSD1(NM_001136042.2):c.915G>A (p.E305=)
ISCN -
DB-ID AARSD1_000011
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00015 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PTGES3L NM_001142653.1 -?/. - c.*12591G>A r.(=) p.(=)
AARSD1 NM_001261434.1 -?/. - c.393G>A r.(?) p.(Glu131=)
PTGES3L-AARSD1 NM_025267.3 -?/. - c.732G>A r.(?) p.(Glu244=)