Variant #0000682435 (NC_000023.10:g.41469236G>A, CASK(NM_003688.3):c.1076C>T)

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.41469236G>A
DNA change (hg38) -
Published as CASK(NM_001126054.2):c.1076C>T (p.(Ala359Val))
ISCN -
DB-ID CASK_000121
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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CASK NM_003688.3 ?/. - c.1076C>T r.(?) p.(Ala359Val)
GPR34 NM_005300.3 ?/. - c.-79198G>A r.(?) p.(=)
GPR82 NM_080817.4 ?/. - c.-114412G>A r.(?) p.(=)