Variant #0001064268 (NC_000004.11:g.153332496C>T, NM_001013415.1:c.-29009G>A (FBXW7))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.153332496C>T
DNA change (hg38) -
Published as FBXW7(NM_001349798.2):c.460G>A (p.(Val154Ile))
ISCN -
DB-ID FBXW7_000023
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) 6.0E-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 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FBXW7 NM_001013415.1 -?/. - c.-29009G>A r.(?) p.(=)
FBXW7 NM_001349798.2 -?/. - c.460G>A r.(?) p.(Val154Ile)
FBXW7 NM_033632.3 -?/. - c.460G>A r.(?) p.(Val154Ile)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.