Variant #0000330563 (NC_000005.9:g.140048191_140048194del, NM_194249.2:c.*2685_*2688del (DND1))

Chromosome 5
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.140048191_140048194del
DNA change (hg38) g.140668606_140668609del
Published as WDR55(NM_017706.4):c.381-7_381-4del (p.?)
ISCN -
DB-ID WDR55_000001
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-17 15:35:50 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WDR55 NM_017706.4 ?/. - c.381-6_381-3del r.spl? p.?
DND1 NM_194249.2 ?/. - c.*2685_*2688del r.(=) p.(=)


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