Variant #0001053500 (NC_000010.10:g.10888024A>G, NM_001025076.2:c.-319276A>G (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.10888024A>G
DNA change (hg38) -
Published as CELF2(NM_001326325.2):c.17-2A>G
ISCN -
DB-ID CELF2_000019
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 2025-11-01 13:22:20 +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.-319276A>G r.(?) p.(=)
CELF2 NM_001025077.2 ?/. - c.-159327A>G r.(?) p.(=)


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