Variant #0001046600 (NC_000017.10:g.18156698_18156699insCTT, NM_002018.3:c.929_930insAAG (FLII))

Chromosome 17
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.18156698_18156699insCTT
DNA change (hg38) -
Published as FLII(NM_001256264.2):c.896_897insAAG (p.S300dup)
ISCN -
DB-ID FLII_000029
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) Retrieve
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FLII NM_002018.3 ?/. - c.929_930insAAG r.(?) p.(Ser311dup)
LLGL1 NM_004140.3 ?/. - c.*9478_*9479insCTT r.(=) p.(=)


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