Variant #0001003701 (NC_000017.10:g.74381722G>T, NM_022066.3:c.*5302C>A (UBE2O))

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.74381722G>T
DNA change (hg38) -
Published as SPHK1(NM_001142601.1):c.-4G>T (p.?)
ISCN -
DB-ID PRPSAP1_000003
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRPSAP1 NM_002766.2 ?/. - c.-31938C>A r.(?) p.(=)
UBE2O NM_022066.3 ?/. - c.*5302C>A r.(=) p.(=)
SPHK1 NM_182965.2 ?/. - c.255G>T r.(?) p.(Glu85Asp)


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