Variant #0000543723 (NC_000011.9:g.2906376A>C, NM_000076.2:c.344T>G (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.2906376A>C
DNA change (hg38) g.2885146A>C
Published as -
ISCN -
DB-ID CDKN1C_000101
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +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.344T>G r.(?) p.(Val115Gly) -
SLC22A18AS NM_007105.2 -?/. - c.*3034T>G r.(=) p.(=) -
SLC22A18 NM_183233.2 -?/. - c.-14793A>C r.(?) p.(=) -


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