Variant #0001027496 (NC_000023.10:g.41390338C>T, NM_003688.3:c.2427G>A (CASK))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.41390338C>T
DNA change (hg38) -
Published as CASK(NM_003688.3):c.2427G>A (p.A809=)
ISCN -
DB-ID CASK_000154
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) 0.00197 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2025-02-07 18:57:27 +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.2427G>A r.(?) p.(Ala809=)
GPR34 NM_005300.3 -?/. - c.-158096C>T r.(?) p.(=)
GPR82 NM_080817.4 -?/. - c.-193310C>T r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.