Variant #0000896228 (NC_000023.10:g.41604776C>T, CASK(NM_003688.3):c.356+1G>A)

Chromosome X
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.41604776C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID CASK_000146
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 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CASK NM_003688.3 +?/. - c.356+1G>A r.spl? p.?
GPR34 NM_005300.3 +?/. - c.*48744C>T r.(=) p.(=)
GPR82 NM_080817.4 +?/. - c.*17486C>T r.(=) p.(=)