Variant #0001033436 (NC_000002.11:g.64114781A>G, NC_000002.11(NM_006759.3):c.1314+3A>G (UGP2))

Chromosome 2
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.64114781A>G
DNA change (hg38) -
Published as UGP2(NM_006759.4):c.1314+3A>G
ISCN -
DB-ID UGP2_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) 9.0E-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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UGP2 NM_006759.3 ?/. - c.1314+3A>G r.spl? p.?
VPS54 NM_016516.2 ?/. - c.*5783T>C r.(=) p.(=)


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