Variant #0001006633 (NC_000023.10:g.18598093G>A, NM_000330.3:c.*62031C>T (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.18598093G>A
DNA change (hg38) -
Published as CDKL5(NM_001037343.1):c.403+5G>A (p.?)
ISCN -
DB-ID RS1_000434
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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RS1 NM_000330.3 ?/. - c.*62031C>T r.(=) p.(=)
CDKL5 NM_003159.2 ?/. - c.403+5G>A r.spl? p.?


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