Variant #0001006756 (NC_000023.10:g.41446204C>T, NM_003688.3:c.1270G>A (CASK))

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.41446204C>T
DNA change (hg38) -
Published as CASK(NM_001367721.1):c.1270G>A (p.(Asp424Asn))
ISCN -
DB-ID CASK_000151
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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +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.1270G>A r.(?) p.(Asp424Asn)
GPR34 NM_005300.3 ?/. - c.-102230C>T r.(?) p.(=)
GPR82 NM_080817.4 ?/. - c.-137444C>T r.(?) p.(=)


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