Variant #0000575138 (NC_000023.10:g.18593605G>T, NM_000330.3:c.*66519C>A (RS1))

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.18593605G>T
DNA change (hg38) g.18575485G>T
Published as CDKL5(NM_003159.3):c.277G>T (p.E93*)
ISCN -
DB-ID RS1_000227
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RS1 NM_000330.3 +/. - c.*66519C>A r.(=) p.(=)
CDKL5 NM_003159.2 +/. - c.277G>T r.(?) p.(Glu93Ter)


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