Variant #0000656773 (NC_000011.9:g.2906192C>G, CDKN1C(NM_000076.2):c.528G>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.2906192C>G
DNA change (hg38) g.2884962C>G
Published as CDKN1C(NM_000076.2):c.528G>C (p.A176=, p.(Ala176=))
ISCN -
DB-ID CDKN1C_000095 See all 5 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) 0.01376 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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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.528G>C r.(?) p.(Ala176=) -
SLC22A18AS NM_007105.2 -?/. - c.*3218G>C r.(=) p.(=) -
SLC22A18 NM_183233.2 -?/. - c.-14977C>G r.(?) p.(=) -