Variant #0000725895 (NC_000016.9:g.67208115G>T, NM_001040715.1:c.*2599C>A (KIAA0895L))

Chromosome 16
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.67208115G>T
DNA change (hg38) -
Published as NOL3(NM_001276312.1):c.43G>T (p.E15*)
ISCN -
DB-ID FBXL8_000009
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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIAA0895L NM_001040715.1 ?/. - c.*2599C>A r.(=) p.(=)
NOL3 NM_001185058.1 ?/. - c.43G>T r.(?) p.(Glu15Ter)
FBXL8 NM_018378.2 ?/. - c.*10392G>T r.(=) p.(=)


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