Variant #0000656771 (NC_000011.9:g.2905985C>T, NM_000076.2:c.735G>A (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.2905985C>T
DNA change (hg38) g.2884755C>T
Published as CDKN1C(NM_000076.2):c.735G>A (p.G245=)
ISCN -
DB-ID CDKN1C_000119
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) 0.00013 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-06-29 16:32:03 +02:00 (CEST)
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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.735G>A r.(?) p.(Gly245=) -
SLC22A18AS NM_007105.2 -?/. - c.*3425G>A r.(=) p.(=) -
SLC22A18 NM_183233.2 -?/. - c.-15184C>T r.(?) p.(=) -


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