Variant #0000275073 (NC_000001.10:g.231829578G>A, NM_018662.2:c.74G>A (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.231829578G>A
DNA change (hg38) g.231693832G>A
Published as DISC1(NM_001164537.1):c.74G>A (p.R25Q)
ISCN -
DB-ID DISC1_000001
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) 0.00057 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-05 20:01:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TSNAX NM_005999.2 -?/. - c.*128927G>A r.(=) p.(=)
DISC1 NM_018662.2 -?/. - c.74G>A r.(?) p.(Arg25Gln)
TSNAX-DISC1 NR_028394.1 -?/. - n.923G>A r.(?) -


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