Variant #0000966322 (NC_000011.9:g.2906165A>G, NM_000076.2:c.555T>C (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.2906165A>G
DNA change (hg38) -
Published as CDKN1C(NM_000076.2):c.537_555delCCCGGCCCCGGCCCCGGCTinsCCCGGCCCCGGCCCCGGCC (p.A179_A185=), CDKN1C(NM_000076.2):c.543_555delCCCGGCCCCGGCTinsCCCGGCCCC...
ISCN -
DB-ID CDKN1C_000068 See all 3 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) 0.22034 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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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.555T>C r.(?) p.(Ala185=) -
SLC22A18AS NM_007105.2 -/. - c.*3245T>C r.(=) p.(=) -
SLC22A18 NM_183233.2 -/. - c.-15004A>G r.(?) p.(=) -


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