Variant #0000371841 (NC_000014.8:g.35182668C>T, NM_138638.4:c.103G>A (CFL2))

Chromosome 14
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.35182668C>T
DNA change (hg38) g.34713462C>T
Published as -
ISCN -
DB-ID CFL2_000001 See all 3 reported entries
Variant remarks pcDNA-DEST cloned; C2C12 normal expression, bacterial expression reduced stability and/or solubility, probable protein misfolding
Reference PubMed: Agrawal 2007, OMIM:var0001
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Alan Beggs
Database submission license No license selected
Created by Alan Beggs
Date created 2009-10-17 20:05:27 +02:00 (CEST)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CFL2 NM_138638.4 +?/. 2 c.103G>A r.(?) p.Ala35Thr


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