Variant #0000576111 (NC_000023.10:g.47088032T>C, CDK16(NM_033018.3):c.1460T>C)

Chromosome X
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.47088032T>C
DNA change (hg38) g.47228633T>C
Published as CDK16(NM_001170460.1):c.1664T>C (p.(Met555Thr))
ISCN -
DB-ID USP11_000022
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) Variant not found in online data sets
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     
USP11 NM_004651.3 -?/. - c.-4282T>C r.(?) p.(=)
CDK16 NM_033018.3 -?/. - c.1460T>C r.(?) p.(Met487Thr)