Variant #0000001675 (NC_000001.11:g.231761122C>T, NC_000001.11(NM_001164537.1):c.1365-6018C>T (DISC1))

Chromosome 1
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.231761122C>T
Published as -
Reference A Talib Norlelawati et al. (2015), dbSNP
DB-ID DISC1_000005 See all 4 reported entries
dbSNP ID rs1538979
Frequency 37/210
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nuur Athirah Binti Mohd Daud
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nuur Athirah Binti Mohd Daud
Date created 2021-01-19 10:22:33 +08:00 (CST)
Date last edited 2021-09-08 10:40:38 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
DISC1 NM_001164537.1 +/. - c.1365-6018C>T - r.(=) p.(=) - -



Screenings

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