Variant #0000859262 (NC_000004.11:g.153332658C>A, NM_001013415.1:c.-29171G>T (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.153332658C>A
DNA change (hg38) -
Published as FBXW7(NM_001349798.2):c.298G>T (p.E100*)
ISCN -
DB-ID FBXW7_000008
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FBXW7 NM_001013415.1 ?/. - c.-29171G>T r.(?) p.(=)
FBXW7 NM_001349798.2 ?/. - c.298G>T r.(?) p.(Glu100*)
FBXW7 NM_033632.3 ?/. - c.298G>T r.(?) p.(Glu100*)


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