Variant #0000693591 (NC_000023.10:g.41448766A>G, CASK(NM_003688.3):c.1233+2T>C)

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.41448766A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID CASK_000124
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2020-09-15 15:50:26 +02:00 (CEST)
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.1233+2T>C r.spl? p.?
GPR34 NM_005300.3 ?/. - c.-99668A>G r.(?) p.(=)
GPR82 NM_080817.4 ?/. - c.-134882A>G r.(?) p.(=)