Variant #0000656772 (NC_000011.9:g.2905994dup, NM_000076.2:c.726dup (CDKN1C))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.2905994dup
DNA change (hg38) g.2884764dup
Published as CDKN1C(NM_000076.2):c.726dupG (p.H243Afs*43)
ISCN -
DB-ID CDKN1C_000120 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-06-29 16:32:16 +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.726dup r.(?) p.(His243AlafsTer43) -
SLC22A18AS NM_007105.2 +/. - c.*3416dup r.(?) p.(=) -
SLC22A18 NM_183233.2 +/. - c.-15175dup r.(?) p.(=) -


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