Variant #0000990958 (NC_000001.10:g.231829752C>T, NM_018662.2:c.248C>T (DISC1))

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.231829752C>T
DNA change (hg38) -
Published as DISC1(NM_001164537.1):c.248C>T (p.(Ala83Val))
ISCN -
DB-ID DISC1_000014
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) 0.0015 View details
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 13:07:21 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TSNAX NM_005999.2 -?/. - c.*129101C>T r.(=) p.(=)
DISC1 NM_018662.2 -?/. - c.248C>T r.(?) p.(Ala83Val)
TSNAX-DISC1 NR_028394.1 -?/. - n.1097C>T r.(?) -


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