Variant #0001056241 (NC_000017.10:g.79862787T>A, NM_002861.3:c.1092A>T (PCYT2))

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.79862787T>A
DNA change (hg38) -
Published as PCYT2(NM_002861.5):c.1092A>T (p.(Glu364Asp))
ISCN -
DB-ID ALYREF_000005
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) 4.0E-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 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     
PCYT2 NM_002861.3 ?/. - c.1092A>T r.(?) p.(Glu364Asp)
ALYREF NM_005782.3 ?/. - c.-13331A>T r.(?) p.(=)
ANAPC11 NM_016476.10 ?/. - c.*4846T>A r.(=) p.(=)
NPB NM_148896.3 ?/. - c.*2163T>A r.(=) p.(=)


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