Variant #0001041673 (NC_000017.10:g.18152096C>G, NC_000017.10(NM_002018.3):c.2018+18G>C (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.18152096C>G
DNA change (hg38) -
Published as FLII(NM_001256264.2):c.1985+18G>C
ISCN -
DB-ID FLII_000027
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) 0.00037 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 2025-05-05 21:14:00 +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.2018+18G>C r.(=) p.(=)
LLGL1 NM_004140.3 -/. - c.*4876C>G r.(=) p.(=)


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