Variant #0000575999 (NC_000023.10:g.41495830C>T, CASK(NM_003688.3):c.915+1G>A)

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.41495830C>T
DNA change (hg38) g.41636577C>T
Published as -
ISCN -
DB-ID CASK_000083
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-19 19:24:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CASK NM_003688.3 +/. - c.915+1G>A r.spl? p.?
GPR34 NM_005300.3 +/. - c.-52604C>T r.(?) p.(=)
GPR82 NM_080817.4 +/. - c.-87818C>T r.(?) p.(=)