Variant #0000998982 (NC_000011.9:g.2906392C>A, NM_000076.2:c.328G>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.2906392C>A
DNA change (hg38) -
Published as CDKN1C(NM_001122630.1):c.295G>T (p.(Ala99Ser))
ISCN -
DB-ID CDKN1C_000149
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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
CDKN1C NM_000076.2 ?/. - c.328G>T r.(?) p.(Ala110Ser) -
SLC22A18AS NM_007105.2 ?/. - c.*3018G>T r.(=) p.(=) -
SLC22A18 NM_183233.2 ?/. - c.-14777C>A r.(?) p.(=) -


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