Variant #0000994125 (NC_000004.11:g.153332894C>T, NM_001013415.1:c.-29407G>A (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.153332894C>T
DNA change (hg38) -
Published as FBXW7(NM_033632.3):c.62G>A (p.(Gly21Asp))
ISCN -
DB-ID FBXW7_000016
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) 3.0E-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 2024-08-28 13:16:32 +02:00 (CEST)
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.-29407G>A r.(?) p.(=)
FBXW7 NM_001349798.2 ?/. - c.62G>A r.(?) p.(Gly21Asp)
FBXW7 NM_033632.3 ?/. - c.62G>A r.(?) p.(Gly21Asp)


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