Variant #0000331074 (NC_000006.11:g.52935905_52935907del, NM_016513.4:c.-9789_-9787del (ICK))

Chromosome 6
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.52935905_52935907del
DNA change (hg38) g.53071107_53071109del
Published as FBXO9(NM_012347.4):c.76_78del (p.(Asp26del))
ISCN -
DB-ID FBXO9_000001
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FBXO9 NM_012347.4 ?/. - c.84_86del r.(?) p.(Asp28del)
ICK NM_016513.4 ?/. - c.-9789_-9787del r.(?) p.(=)


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