Variant #0000558714 (NC_000016.9:g.67208570G>C, NM_001040715.1:c.*2144C>G (KIAA0895L))

Chromosome 16
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.67208570G>C
DNA change (hg38) g.67174667G>C
Published as NOL3(NM_001185057.2):c.332G>C (p.R111P)
ISCN -
DB-ID FBXL8_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) 0.00054 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIAA0895L NM_001040715.1 -?/. - c.*2144C>G r.(=) p.(=)
NOL3 NM_001185058.1 -?/. - c.342G>C r.(?) p.(Thr114=)
FBXL8 NM_018378.2 -?/. - c.*10847G>C r.(=) p.(=)


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