Variant #0000604824 (NC_000001.10:g.152327158_152327161del, NM_002016.1:c.-29518_-29515del (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.152327158_152327161del
DNA change (hg38) g.152354682_152354685del
Published as FLG2(NM_001014342.3):c.3101_3104delAATA (p.Q1034Pfs*192)
ISCN -
DB-ID FLG_000347
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) 0.00077 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 14:54:23 +01:00 (CET)
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.3101_3104del r.(?) p.(Gln1034ProfsTer192)
FLG NM_002016.1 ?/. - c.-29518_-29515del r.(?) p.(=)


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