Variant #0000321967 (NC_000011.9:g.2909513C>G, CDKN1C(NM_000076.2):c.-2794G>C)

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.2909513C>G
DNA change (hg38) g.2888283C>G
Published as SLC22A18AS(NM_007105.2):c.659G>C (p.(Arg220Pro))
ISCN -
DB-ID SLC22A18AS_000006
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) 0.00744 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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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.-2794G>C r.(?) p.(=) -
SLC22A18AS NM_007105.2 -?/. - c.659G>C r.(?) p.(Arg220Pro) -
SLC22A18 NM_183233.2 -?/. - c.-11656C>G r.(?) p.(=) -