Variant #0000998119 (NC_000010.10:g.11312752A>C, NM_001025076.2:c.649A>C (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.11312752A>C
DNA change (hg38) -
Published as CELF2(NM_006561.3):c.742A>C (p.(Thr248Pro))
ISCN -
DB-ID CELF2_000013
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 2024-08-28 13:16:32 +02:00 (CEST)
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.649A>C r.(?) p.(Thr217Pro)
CELF2 NM_001025077.2 ?/. - c.721A>C r.(?) p.(Thr241Pro)


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