Variant #0000333901 (NC_000023.10:g.47082616C>G, CDK16(NM_033018.3):c.13-335C>G)

Chromosome X
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.47082616C>G
DNA change (hg38) g.47223217C>G
Published as CDK16(NM_001170460.1):c.122C>G (p.(Ala41Gly))
ISCN -
DB-ID CDK16_000007
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00137 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDK16 NM_033018.3 ?/. - c.13-335C>G r.(=) p.(=)