Variant #0000619566 (NC_000023.10:g.41390265G>A, CASK(NM_003688.3):c.2500C>T)

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.41390265G>A
DNA change (hg38) g.41531012G>A
Published as CASK(NM_001126054.2):c.2431C>T (p.(Pro811Ser))
ISCN -
DB-ID CASK_000087 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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
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.2500C>T r.(?) p.(Pro834Ser)
GPR34 NM_005300.3 -?/. - c.-158169G>A r.(?) p.(=)
GPR82 NM_080817.4 -?/. - c.-193383G>A r.(?) p.(=)