Variant #0001068413 (NC_000004.11:g.153244092G>A, NM_001349798.2:c.2065C>T (FBXW7))

Chromosome 4
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.153244092G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID FBXW7_000002 See all 5 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2126459661
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-02-19 14:16:01 +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     
FBXW7 NM_001349798.2 +/. - c.2065C>T r.(?) p.(Arg689Trp)


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