Variant #0000980928 (NC_000014.8:g.51372187G>A, NM_002863.4:c.2467C>T (PYGL))

Chromosome 14
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.51372187G>A
DNA change (hg38) -
Published as PYGL(NM_002863.5):c.2467C>T (p.(Gln823Ter))
ISCN -
DB-ID PYGL_000017 See all 14 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) 6.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABHD12B NM_001206673.1 +/. - c.*1103G>A r.(=) p.(=)
PYGL NM_002863.4 +/. - c.2467C>T r.(?) p.(Gln823*)


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