Variant #0000990334 (NC_000001.10:g.152285789C>T, NM_002016.1:c.1573G>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.152285789C>T
DNA change (hg38) -
Published as FLG(NM_002016.1):c.1573G>A (p.(Gly525Arg))
ISCN -
DB-ID FLG_000637
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) 0.00037 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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FLG2 NM_001014342.2 -?/. - c.*37297G>A r.(=) p.(=)
FLG NM_002016.1 -?/. - c.1573G>A r.(?) p.(Gly525Arg)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.