Variant #0000682436 (NC_000023.10:g.41587109A>G, NC_000023.10(NM_003688.3):c.429+11528T>C (CASK))

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.41587109A>G
DNA change (hg38) -
Published as GPR82(NM_080817.4):c.830A>G (p.Q277R)
ISCN -
DB-ID CASK_000122
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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CASK NM_003688.3 -?/. - c.429+11528T>C r.(=) p.(=)
GPR34 NM_005300.3 -?/. - c.*31077A>G r.(=) p.(=)
GPR82 NM_080817.4 -?/. - c.830A>G r.(?) p.(Gln277Arg)


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