Variant #0000928873 (NC_000004.11:g.153332617_153332619del, NM_001013415.1:c.-29120_-29118del (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.153332617_153332619del
DNA change (hg38) -
Published as FBXW7(NM_033632.3):c.349_351delGAG (p.E117del)
ISCN -
DB-ID FBXW7_000011
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-07-07 10:10:56 +02:00 (CEST)
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_001013415.1 ?/. - c.-29120_-29118del r.(?) p.(=)
FBXW7 NM_001349798.2 ?/. - c.349_351del r.(?) p.(Glu117del)
FBXW7 NM_033632.3 ?/. - c.349_351del r.(?) p.(Glu117del)


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