Variant #0000503460 (NC_000001.10:g.152326322_152326323dup, NM_002016.1:c.-28680_-28679dup (FLG))

Chromosome 1
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.152326322_152326323dup
DNA change (hg38) g.152353846_152353847dup
Published as FLG2(NM_001014342.3):c.3939_3940dup (p.(Thr1314IlefsTer223)), FLG2(NM_001014342.3):c.3939_3940dupTA (p.T1314Ifs*223)
ISCN -
DB-ID FLG_000326 See all 2 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:20:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FLG2 NM_001014342.2 ?/. - c.3939_3940dup r.(?) p.(Thr1314IlefsTer223)
FLG NM_002016.1 ?/. - c.-28680_-28679dup r.(?) p.(=)


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