Variant #0000503449 (NC_000001.10:g.152285868C>G, NM_002016.1:c.1494G>C (FLG))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.152285868C>G
DNA change (hg38) g.152313392C>G
Published as FLG(NM_002016.1):c.1494G>C (p.E498D, p.(Glu498Asp))
ISCN -
DB-ID FLG_000316 See all 2 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) 0.0019 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 14:54:23 +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.*37218G>C r.(=) p.(=)
FLG NM_002016.1 -/. - c.1494G>C r.(?) p.(Glu498Asp)


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