Variant #0000269762 (NC_000023.10:g.41530667del, CASK(NM_003688.3):c.532+25del)

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.41530667del
DNA change (hg38) g.41671414del
Published as CASK(NM_003688.3):c.532+25delA
ISCN -
DB-ID CASK_000040
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CASK NM_003688.3 -/. - c.532+25del r.(=) p.(=)
GPR34 NM_005300.3 -/. - c.-17767del r.(?) p.(=)
GPR82 NM_080817.4 -/. - c.-52981del r.(?) p.(=)