Variant #0000994124 (NC_000004.11:g.153273882T>A, NC_000004.11(NM_001013415.1):c.148-2606A>T (FBXW7))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.153273882T>A
DNA change (hg38) -
Published as FBXW7(NM_018315.4):c.1A>T (p.(Met1?))
ISCN -
DB-ID FBXW7_000015
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) 0 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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FBXW7 NM_001013415.1 -?/. - c.148-2606A>T r.(=) p.(=)
FBXW7 NM_001349798.2 -?/. - c.502-2606A>T r.(=) p.(=)
FBXW7 NM_033632.3 -?/. - c.502-2606A>T r.(=) p.(=)


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