Variant #0000269761 (NC_000023.10:g.41530666T>A, CASK(NM_003688.3):c.532+15A>T)

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.41530666T>A
DNA change (hg38) g.41671413T>A
Published as CASK(NM_003688.3):c.532+15A>T
ISCN -
DB-ID CASK_000041
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 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CASK NM_003688.3 -?/. - c.532+15A>T r.(=) p.(=)
GPR34 NM_005300.3 -?/. - c.-17768T>A r.(?) p.(=)
GPR82 NM_080817.4 -?/. - c.-52982T>A r.(?) p.(=)