Variant #0000949648 (NC_000011.9:g.2905241A>G, NM_000076.2:c.944T>C (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.2905241A>G
DNA change (hg38) -
Published as CDKN1C(NM_000076.2):c.944T>C (p.(Leu315Pro))
ISCN -
DB-ID CDKN1C_000142
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 2023-11-27 17:35:39 +01:00 (CET)
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.944T>C r.(?) p.(Leu315Pro) -
SLC22A18AS NM_007105.2 -?/. - c.*4169T>C r.(=) p.(=) -
SLC22A18 NM_183233.2 -?/. - c.-15928A>G r.(?) p.(=) -


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