Variant #0001051389 (NC_000003.11:g.62358208_62358213dup, NM_018008.3:c.342_347dup (FEZF2))

Chromosome 3
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.62358208_62358213dup
DNA change (hg38) -
Published as FEZF2(NM_018008.4):c.342_347dup (p.(Gly116_Gly117dup))
ISCN -
DB-ID FEZF2_000002
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     
FEZF2 NM_018008.3 ?/. - c.342_347dup r.(?) p.(Gly116_Gly117dup)


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