Variant #0000947942 (NC_000002.11:g.48132756_48132782del, NM_001190274.1:c.83_109del (FBXO11))

Chromosome 2
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.48132756_48132782del
DNA change (hg38) -
Published as FBXO11(NM_001190274.2):c.83_109delCGCAGCAGCCGCCGCCGCAGCCGCCCC (p.P28_P36del)
ISCN -
DB-ID FBXO11_000047
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 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FBXO11 NM_001190274.1 ?/. - c.83_109del r.(?) p.(Pro28_Pro36del)


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