Variant #0000575985 (NC_000023.10:g.41383310_41383311dup, CASK(NM_003688.3):c.2506-12_2506-11dup)

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.41383310_41383311dup
DNA change (hg38) g.41524057_41524058dup
Published as CASK(NM_003688.3):c.2506-12_2506-11dupTT
ISCN -
DB-ID CASK_000075
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 2019-07-18 18:22:55 +02:00 (CEST)
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.2506-12_2506-11dup r.(=) p.(=)
GPR34 NM_005300.3 -/. - c.-165124_-165123dup r.(?) p.(=)
GPR82 NM_080817.4 -/. - c.-200338_-200337dup r.(?) p.(=)