Variant #0000658041 (NC_000017.10:g.16221214C>T, NM_004278.3:c.652C>T (PIGL))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.16221214C>T
DNA change (hg38) g.16317900C>T
Published as PIGL(NM_004278.3):c.652C>T (p.Q218*), PIGL(NM_004278.4):c.652C>T (p.(Gln218*))
ISCN -
DB-ID PIGL_000003 See all 3 reported entries
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PIGL NM_004278.3 +/. - c.652C>T r.(?) p.(Gln218Ter)


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