Variant #0001044332 (NC_000023.10:g.41470966T>A, NC_000023.10(NM_003688.3):c.1034-1688A>T (CASK))

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.41470966T>A
DNA change (hg38) -
Published as CASK(NM_001367721.1):c.1034-1688A>T
ISCN -
DB-ID CASK_000155
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
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.1034-1688A>T r.(=) p.(=)
GPR34 NM_005300.3 -?/. - c.-77468T>A r.(?) p.(=)
GPR82 NM_080817.4 -?/. - c.-112682T>A r.(?) p.(=)


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