Variant #0000321427 (NC_000010.10:g.11367916_11367919del, NM_001025076.2:c.1319_1322del (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.11367916_11367919del
DNA change (hg38) g.11325953_11325956del
Published as CELF2(NM_006561.3):c.1409_1412del (p.(Lys471ArgfsTer4))
ISCN -
DB-ID CELF2_000002
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-02-08 18:36:18 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CELF2 NM_001025076.2 ?/. - c.1319_1322del r.(?) p.(Lys440ArgfsTer4)
CELF2 NM_001025077.2 ?/. - c.1373_1376del r.(?) p.(Lys458ArgfsTer4)


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