Variant #0000321951 (NC_000011.9:g.2905369G>A, NC_000011.9(NM_000076.2):c.821-5C>T (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.2905369G>A
DNA change (hg38) g.2884139G>A
Published as CDKN1C(NM_000076.2):c.821-5C>T (p.?)
ISCN -
DB-ID CDKN1C_000061
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) 0.0004 View details
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 2020-06-29 16:31:47 +02:00 (CEST)
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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.821-5C>T r.spl? p.? -
SLC22A18AS NM_007105.2 -?/. - c.*4041C>T r.(=) p.(=) -
SLC22A18 NM_183233.2 -?/. - c.-15800G>A r.(?) p.(=) -


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