Variant #0000503462 (NC_000001.10:g.152327469_152327699del, NM_002016.1:c.-30024_-29794del (FLG))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.152327469_152327699del
DNA change (hg38) g.152354993_152355223del
Published as FLG2(NM_001014342.2):c.2595_2825del (p.(Ser869_Thr945del)), FLG2(NM_001014342.3):c.2595_2825del (p.S869_T945del)
ISCN -
DB-ID FLG_000328 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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
FLG2 NM_001014342.2 -?/. - c.2595_2825del r.(?) p.(Ser869_Thr945del)
FLG NM_002016.1 -?/. - c.-30024_-29794del r.(?) p.(=)


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