Variant #0001006757 (NC_000023.10:g.41586722A>T, NC_000023.10(NM_003688.3):c.429+11915T>A (CASK))

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.41586722A>T
DNA change (hg38) -
Published as GPR82(NM_080817.4):c.443A>T (p.(Gln148Leu))
ISCN -
DB-ID CASK_000152
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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CASK NM_003688.3 ?/. - c.429+11915T>A r.(=) p.(=)
GPR34 NM_005300.3 ?/. - c.*30690A>T r.(=) p.(=)
GPR82 NM_080817.4 ?/. - c.443A>T r.(?) p.(Gln148Leu)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.