Variant #0000321954 (NC_000011.9:g.2906108_2906119del, NM_000076.2:c.618_629del (CDKN1C))

Chromosome 11
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.2906108_2906119del
DNA change (hg38) g.2884878_2884889del
Published as CDKN1C(NM_000076.2):c.618_629del (p.(Ala213_Pro216del)), CDKN1C(NM_000076.2):c.618_629delGGCCCCGGCCCC (p.A213_P216del)
ISCN -
DB-ID CDKN1C_000048 See all 5 reported entries
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
CDKN1C NM_000076.2 -?/. - c.618_629del r.(?) p.(Ala213_Pro216del) -
SLC22A18AS NM_007105.2 -?/. - c.*3308_*3319del r.(=) p.(=) -
SLC22A18 NM_183233.2 -?/. - c.-15061_-15050del r.(?) p.(=) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.