Variant #0000896227 (NC_000023.10:g.41437631G>A, CASK(NM_003688.3):c.1465C>T)

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.41437631G>A
DNA change (hg38) -
Published as CASK(NM_001367721.1):c.1465C>T (p.R489W)
ISCN -
DB-ID CASK_000145
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 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CASK NM_003688.3 +/. - c.1465C>T r.(?) p.(Arg489Trp)
GPR34 NM_005300.3 +/. - c.-110803G>A r.(?) p.(=)
GPR82 NM_080817.4 +/. - c.-146017G>A r.(?) p.(=)