Variant #0000371832 (NC_000014.8:g.35184228C>T, NM_138638.4:c.-482G>A (CFL2))

Chromosome 14
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.35184228C>T
DNA change (hg38) g.34715022C>T
Published as -
ISCN -
DB-ID CFL2_000011
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs17525727
Origin Germline
Segregation -
Frequency 0.16-0.18
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Ivo F.A.C. Fokkema
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2009-12-05 11:40:56 +01:00 (CET)
Date last edited 2012-11-03 11:45:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CFL2 NM_138638.4 ?/. _1 c.-482G>A r.(=) p.(=)


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