Variant #0000273071 (NC_000011.9:g.2906012C>T, NM_000076.2:c.708G>A (CDKN1C))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.2906012C>T
DNA change (hg38) g.2884782C>T
Published as CDKN1C(NM_000076.2):c.708G>A (p.E236=, p.(Glu236=))
ISCN -
DB-ID CDKN1C_000062 See all 2 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) 0.00387 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-05-09 15:51:19 +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.708G>A r.(?) p.(Glu236=) -
SLC22A18AS NM_007105.2 -/. - c.*3398G>A r.(=) p.(=) -
SLC22A18 NM_183233.2 -/. - c.-15157C>T r.(?) p.(=) -


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