Variant #0000543703 (NC_000011.9:g.2906085_2906186del, NM_000076.2:c.548_649del (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.2906085_2906186del
DNA change (hg38) g.2884855_2884956del
Published as CDKN1C(NM_000076.2):c.548_649del (p.(Ala183_Pro216del))
ISCN -
DB-ID CDKN1C_000088
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 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.548_649del r.(?) p.(Ala183_Pro216del) -
SLC22A18AS NM_007105.2 -?/. - c.*3238_*3339del r.(=) p.(=) -
SLC22A18 NM_183233.2 -?/. - c.-15084_-14983del r.(?) p.(=) -


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