Variant #0001024895 (NC_000004.11:g.153244136C>G, NM_001013415.1:c.1667G>C (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.153244136C>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID FBXW7_000018
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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2025-02-07 18:57:27 +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.1667G>C r.(?) p.(Arg556Pro)
FBXW7 NM_001349798.2 +/. - c.2021G>C r.(?) p.(Arg674Pro)
FBXW7 NM_033632.3 +/. - c.2021G>C r.(?) p.(Arg674Pro)


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