Variant #0000280821 (NC_000001.10:g.152285081_152285084del, NM_002016.1:c.2282_2285del (FLG))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.152285081_152285084del
DNA change (hg38) g.152312605_152312608del
Published as FLG(NM_002016.1):c.2282_2285delCAGT (p.S761Cfs*36), FLG(NM_002016.2):c.2282_2285del (p.(Ser761CysfsTer36)), FLG(NM_002016.2):c.2282_2285delCAGT (p...)
ISCN -
DB-ID FLG_000076 See all 8 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 2018-01-15 20:58:59 +01:00 (CET)
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.*38006_*38009del r.(=) p.(=)
FLG NM_002016.1 +/. - c.2282_2285del r.(?) p.(Ser761CysfsTer36)


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