Variant #0001034382 (NC_000004.11:g.153249481T>A, NM_001013415.1:c.943A>T (FBXW7))

Chromosome 4
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.153249481T>A
DNA change (hg38) -
Published as FBXW7(NM_001349798.2):c.1297A>T (p.(Ile433Phe))
ISCN -
DB-ID FBXW7_000019
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) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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     
FBXW7 NM_001013415.1 ?/. - c.943A>T r.(?) p.(Ile315Phe)
FBXW7 NM_001349798.2 ?/. - c.1297A>T r.(?) p.(Ile433Phe)
FBXW7 NM_033632.3 ?/. - c.1297A>T r.(?) p.(Ile433Phe)


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