Variant #0000716856 (NC_000001.10:g.152285186_152285192del, NM_002016.1:c.2175_2181del (FLG))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.152285186_152285192del
DNA change (hg38) -
Published as FLG(NM_002016.2):c.2175_2181delTGGGCAC (p.G726Dfs*70)
ISCN -
DB-ID FLG_000305
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FLG2 NM_001014342.2 +?/. - c.*37899_*37905del r.(=) p.(=)
FLG NM_002016.1 +?/. - c.2175_2181del r.(?) p.(Gly726AspfsTer70)


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