Variant #0000574993 (NC_000023.10:g.154005109_154005111dup, NM_001363.3:c.1512_1514dup (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.154005109_154005111dup
DNA change (hg38) g.154776834_154776836dup
Published as DKC1(NM_001142463.1):c.1497_1499dup (p.(Lys500dup)), DKC1(NM_001363.3):c.1512_1514dupGAA (p.K505dup), DKC1(NM_001363.5):c.1512_1514dupGAA (p.K505dup)
ISCN -
DB-ID DKC1_000092 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) 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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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.1512_1514dup r.(?) p.(Lys505dup) -
MPP1 NM_002436.3 ?/. - c.*2361_*2363dup r.(=) p.(=) -


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