Variant #0000268692 (NC_000023.10:g.154005106_154005111del, NM_001363.3:c.1509_1514del (DKC1))

Chromosome X
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.154005106_154005111del
DNA change (hg38) g.154776831_154776836del
Published as DKC1(NM_001363.3):c.1509_1514delGAAGAA (p.K504_K505del)
ISCN -
DB-ID DKC1_000077
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
DKC1 NM_001363.3 -?/. - c.1509_1514del r.(?) p.(Lys504_Lys505del) -
MPP1 NM_002436.3 -?/. - c.*2358_*2363del r.(=) p.(=) -


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