Variant #0000561553 (NC_000017.10:g.41131677C>G, PTGES3L-AARSD1(NM_025267.3):c.-43G>C)

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.41131677C>G
DNA change (hg38) g.42979660C>G
Published as PTGES3L(NM_001261430.1):c.141G>C (p.Q47H), PTGES3L-AARSD1(NM_001136042.2):c.141G>C (p.Q47H)
ISCN -
DB-ID AARSD1_000009
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) Retrieve
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.141G>C r.(?) p.(Gln47His)
AARSD1 NM_001261434.1 ?/. - c.-15220G>C r.(?) p.(=)
PTGES3L-AARSD1 NM_025267.3 ?/. - c.-43G>C r.(?) p.(=)
RUNDC1 NM_173079.2 ?/. - c.-917C>G r.(?) p.(=)