Variant #0000810393 (NC_000023.10:g.41485880A>G, CASK(NM_003688.3):c.992T>C)

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.41485880A>G
DNA change (hg38) -
Published as CASK(NM_001367721.1):c.992T>C (p.F331S)
ISCN -
DB-ID CASK_000138
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
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.992T>C r.(?) p.(Phe331Ser)
GPR34 NM_005300.3 ?/. - c.-62554A>G r.(?) p.(=)
GPR82 NM_080817.4 ?/. - c.-97768A>G r.(?) p.(=)