Variant #0001003021 (NC_000017.10:g.18137152_18137154del, NM_002018.3:c.*11301_*11303del (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.18137152_18137154del
DNA change (hg38) -
Published as LLGL1(NM_004140.3):c.453_455delAGC (p.(Ala152del))
ISCN -
DB-ID FLII_000014
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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.*11301_*11303del r.(=) p.(=)
LLGL1 NM_004140.3 ?/. - c.453_455del r.(?) p.(Ala152del)


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