Variant #0000612298 (NC_000010.10:g.11371008C>T, NM_001025076.2:c.1465C>T (CELF2))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.11371008C>T
DNA change (hg38) g.11329045C>T
Published as CELF2(NM_001025077.2):c.1519C>T (p.P507S)
ISCN -
DB-ID CELF2_000006 See all 3 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CELF2 NM_001025076.2 +?/. - c.1465C>T r.(?) p.(Pro489Ser)
CELF2 NM_001025077.2 +?/. - c.1519C>T r.(?) p.(Pro507Ser)


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