Variant #0000552739 (NC_000014.8:g.59112874G>A, NM_016651.5:c.1533G>A (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.59112874G>A
DNA change (hg38) g.58646156G>A
Published as DACT1(NM_016651.5):c.1533G>A (p.Q511=), DACT1(NM_016651.6):c.1533G>A (p.Q511=)
ISCN -
DB-ID DACT1_000010 See all 2 reported entries
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) 4.0E-5 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 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DACT1 NM_016651.5 -?/. - c.1533G>A r.(?) p.(Gln511=)


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