Variant #0000269755 (NC_000023.10:g.41412957C>T, CASK(NM_003688.3):c.2039+15G>A)

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.41412957C>T
DNA change (hg38) g.41553704C>T
Published as CASK(NM_003688.3):c.2039+15G>A
ISCN -
DB-ID CASK_000031
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) 0.00156 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.2039+15G>A r.(=) p.(=)
GPR34 NM_005300.3 -?/. - c.-135477C>T r.(?) p.(=)
GPR82 NM_080817.4 -?/. - c.-170691C>T r.(?) p.(=)