Variant #0000798797 (NC_000001.10:g.152324432C>T, NM_002016.1:c.-26789G>A (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.152324432C>T
DNA change (hg38) -
Published as FLG2(NM_001014342.3):c.5830G>A (p.G1944R)
ISCN -
DB-ID FLG_000497
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) 0.00019 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 2021-09-17 14:40:49 +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.5830G>A r.(?) p.(Gly1944Arg)
FLG NM_002016.1 ?/. - c.-26789G>A r.(?) p.(=)


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