Variant #0000575137 (NC_000023.10:g.18593522G>A, RS1(NM_000330.3):c.*66602C>T)

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.18593522G>A
DNA change (hg38) g.18575402G>A
Published as CDKL5(NM_001323289.2):c.194G>A (p.R65Q)
ISCN -
DB-ID CDKL5_000011 See all 2 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) 2.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RS1 NM_000330.3 ?/. - c.*66602C>T r.(=) p.(=)
CDKL5 NM_003159.2 ?/. - c.194G>A r.(?) p.(Arg65Gln)