Variant #0000912071 (NC_000004.11:g.153244137G>T, NM_001013415.1:c.1666C>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.153244137G>T
DNA change (hg38) -
Published as FBXW7(NM_033632.3):c.2020C>A (p.R674=)
ISCN -
DB-ID FBXW7_000009 See all 2 reported entries
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) 0.00058 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 2023-01-11 15:44:22 +01:00 (CET)
Date last edited 2026-01-20 18:57:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FBXW7 NM_001013415.1 -?/. - c.1666C>A r.(?) p.(Arg556=)
FBXW7 NM_001349798.2 -?/. - c.2020C>A r.(?) p.(Arg674=)
FBXW7 NM_033632.3 -?/. - c.2020C>A r.(?) p.(Arg674=)


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