Variant #0000913566 (NC_000011.9:g.2905968G>A, NM_000076.2:c.752C>T (CDKN1C))

Chromosome 11
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.2905968G>A
DNA change (hg38) -
Published as CDKN1C(NM_000076.2):c.752C>T (p.A251V)
ISCN -
DB-ID CDKN1C_000137
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
CDKN1C NM_000076.2 ?/. - c.752C>T r.(?) p.(Ala251Val) -
SLC22A18AS NM_007105.2 ?/. - c.*3442C>T r.(=) p.(=) -
SLC22A18 NM_183233.2 ?/. - c.-15201G>A r.(?) p.(=) -


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