Variant #0000726002 (NC_000016.9:g.84199566G>T, NC_000016.9(NM_178452.4):c.1030+11G>T (DNAAF1))

Chromosome 16
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.84199566G>T
DNA change (hg38) -
Published as DNAAF1(NM_001318756.1):c.285G>T (p.S95=)
ISCN -
DB-ID DNAAF1_000052
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAF1C NM_005679.3 -?/. - c.*12981C>A r.(=) p.(=)
DNAAF1 NM_178452.4 -?/. - c.1030+11G>T r.(=) p.(=)


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