Variant #0000291966 (NC_000023.10:g.154007604_154007606del, NM_001363.3:c.*2462_*2464del (DKC1))

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.154007604_154007606del
DNA change (hg38) g.154779329_154779331del
Published as MPP1(NM_001166462.1):c.1159_1161delAAG (p.K387del)
ISCN -
DB-ID MPP1_000007
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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.*2462_*2464del r.(=) p.(=) -
MPP1 NM_002436.3 ?/. - c.1249_1251del r.(?) p.(Lys417del) -


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