Variant #0001078060 (NC_000014.8:g.59113231G>T, NM_016651.5:c.1890G>T (DACT1))

Chromosome 14
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.59113231G>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID DACT1_000012 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs201251394
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00047 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-05-21 12:02:01 +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     
DACT1 NM_016651.5 -?/. - c.1890G>T r.(?) p.(Lys630Asn)


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