Variant #0001046599 (NC_000017.10:g.18148534C>T, NM_002018.3:c.3728G>A (FLII))

Chromosome 17
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.18148534C>T
DNA change (hg38) -
Published as FLII(NM_001256264.2):c.3695G>A (p.R1232H)
ISCN -
DB-ID FLII_000028
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) 0.01768 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2025-07-08 13:22:38 +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     
FLII NM_002018.3 -/. - c.3728G>A r.(?) p.(Arg1243His)
LLGL1 NM_004140.3 -/. - c.*1314C>T r.(=) p.(=)


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