Variant #0000575994 (NC_000023.10:g.41448750A>G, CASK(NM_003688.3):c.1233+18T>C)

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.41448750A>G
DNA change (hg38) g.41589497A>G
Published as CASK(NM_003688.3):c.1233+18T>C
ISCN -
DB-ID CASK_000069 See all 2 reported entries
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) 0.00063 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.1233+18T>C r.(=) p.(=)
GPR34 NM_005300.3 -/. - c.-99684A>G r.(?) p.(=)
GPR82 NM_080817.4 -/. - c.-134898A>G r.(?) p.(=)