Variant #0000809819 (NC_000023.10:g.118971901C>T, NM_080632.2:c.1121G>A (UPF3B))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.118971901C>T
DNA change (hg38) -
Published as UPF3B(NM_023010.3):c.1082G>A (p.(Arg361His)), UPF3B(NM_080632.2):c.1121G>A (p.R374H)
ISCN -
DB-ID UPF3B_000010 See all 3 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) 0.0005 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +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     
UPF3B NM_080632.2 -?/. - c.1121G>A r.(?) p.(Arg374His)


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