Variant #0000502595 (NC_000001.10:g.116243877_116243879del, NM_001232.3:c.1185_1187del (CASQ2))

Chromosome 1
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.116243877_116243879del
DNA change (hg38) g.115701256_115701258del
Published as CASQ2(NM_001232.3):c.1185_1187delCGA (p.D398del), CASQ2(NM_001232.4):c.1185_1187delCGA (p.D398del)
ISCN -
DB-ID CASQ2_000024 See all 6 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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CASQ2 NM_001232.3 -?/. - c.1185_1187del r.(?) p.(Asp398del)
VANGL1 NM_138959.2 -?/. - c.*9877_*9879del r.(=) p.(=)


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