Variant #0001050482 (NC_000001.10:g.235969981C>T, NM_000081.3:c.2455G>A (LYST))

Chromosome 1
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.235969981C>T
DNA change (hg38) -
Published as LYST(NM_000081.4):c.2455G>A (p.(Ala819Thr)), LYST(NM_001301365.1):c.2455G>A (p.A819T)
ISCN -
DB-ID LYST_000159 See all 2 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) 0.0001 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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LYST NM_000081.3 ?/. - c.2455G>A r.(?) p.(Ala819Thr)


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