Variant #0000722689 (NC_000010.10:g.11363319_11363334dup, NM_001025076.2:c.1171_1186dup (CELF2))

Chromosome 10
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.11363319_11363334dup
DNA change (hg38) -
Published as CELF2(NM_001025077.3):c.1225_1240dupCAGCAGAGCGCTGCAG (p.G414Afs*45)
ISCN -
DB-ID CELF2_000004
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CELF2 NM_001025076.2 ?/. - c.1171_1186dup r.(?) p.(Gly396AlafsTer45)
CELF2 NM_001025077.2 ?/. - c.1225_1240dup r.(?) p.(Gly414AlafsTer45)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.