Variant #0000505909 (NC_000001.10:g.231830364C>T, NM_018662.2:c.860C>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.231830364C>T
DNA change (hg38) g.231694618C>T
Published as DISC1(NM_001164537.1):c.860C>T (p.P287L)
ISCN -
DB-ID DISC1_000011
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) 0.00095 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-05 20:01:26 +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.*129713C>T r.(=) p.(=)
DISC1 NM_018662.2 -?/. - c.860C>T r.(?) p.(Pro287Leu)
TSNAX-DISC1 NR_028394.1 -?/. - n.1709C>T r.(?) -


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