Variant #0000990339 (NC_000001.10:g.152286804G>T, NM_002016.1:c.558C>A (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.152286804G>T
DNA change (hg38) -
Published as FLG(NM_002016.1):c.558C>A (p.(Asn186Lys))
ISCN -
DB-ID FLG_000642
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) 2.0E-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 2024-08-28 13:07:21 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FLG2 NM_001014342.2 -?/. - c.*36282C>A r.(=) p.(=)
FLG NM_002016.1 -?/. - c.558C>A r.(?) p.(Asn186Lys)


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