Variant #0001050476 (NC_000001.10:g.231954115del, NM_018662.2:c.1833del (DISC1))

Chromosome 1
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.231954115del
DNA change (hg38) -
Published as DISC1(NM_018662.3):c.1833del (p.(Arg612Aspfs*3))
ISCN -
DB-ID DISC1_000015
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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TSNAX NM_005999.2 ?/. - c.*253464del r.(?) p.(=)
DISC1 NM_018662.2 ?/. - c.1833del r.(?) p.(Arg612Aspfs*3)
DISC2 NR_002227.2 ?/. - n.150del r.(?) -
TSNAX-DISC1 NR_028394.1 ?/. - n.2682del r.(?) -


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