Variant #0001002622 (NC_000016.9:g.84213952T>C, NM_178452.4:c.*2505T>C (DNAAF1))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.84213952T>C
DNA change (hg38) -
Published as TAF1C(NM_001243156.1):c.1309-2A>G (p.?)
ISCN -
DB-ID DNAAF1_000065
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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
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.1387-2A>G r.spl? p.?
DNAAF1 NM_178452.4 ?/. - c.*2505T>C r.(=) p.(=)


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