Variant #0000615156 (NC_000014.8:g.99976589dup, NM_001099402.1:c.1213dup (CCNK))

Chromosome 14
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.99976589dup
DNA change (hg38) g.99510252dup
Published as CCNK(NM_001099402.1):c.1213dup (p.(Ala405GlyfsTer179))
ISCN -
DB-ID CCNK_000008
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-05 16:49:46 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCNK NM_001099402.1 -?/. - c.1213dup r.(?) p.(Ala405GlyfsTer179)
CCDC85C NM_001144995.1 -?/. - c.*4995dup r.(?) p.(=)


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