Variant #0000333326 (NC_000023.10:g.18646629_18646630del, NM_000330.3:c.*13494_*13495del (RS1))

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.18646629_18646630del
DNA change (hg38) g.18628509_18628510del
Published as CDKL5(NM_001037343.1):c.2635_2636del (p.(Leu879GlufsTer30))
ISCN -
DB-ID CDKL5_000058 See all 3 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_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 2020-07-17 19:47:05 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RS1 NM_000330.3 ?/. - c.*13494_*13495del r.(=) p.(=)
CDKL5 NM_003159.2 ?/. - c.2635_2636del r.(?) p.(Leu879GlufsTer30)


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