Variant #0000895897 (NC_000023.10:g.118975174_118975177del, NM_080632.2:c.674_677del (UPF3B))

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.118975174_118975177del
DNA change (hg38) -
Published as UPF3B(NM_080632.2):c.674_677delGAAA (p.R225Kfs*22), UPF3B(NM_080632.3):c.674_677delGAAA (p.R225Kfs*22)
ISCN -
DB-ID UPF3B_000002 See all 4 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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UPF3B NM_080632.2 +/. - c.674_677del r.(?) p.(Arg225Lysfs*22)


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