Variant #0000914749 (NC_000017.10:g.18148485G>A, NM_002018.3:c.3777C>T (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.18148485G>A
DNA change (hg38) -
Published as FLII(NM_001256264.2):c.3744C>T (p.H1248=)
ISCN -
DB-ID FLII_000008
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) 0.24953 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 2023-01-11 15:44:22 +01:00 (CET)
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.3777C>T r.(?) p.(His1259=)
LLGL1 NM_004140.3 -/. - c.*1265G>A r.(=) p.(=)


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