Variant #0000324949 (NC_000016.9:g.84213242_84213254del, NM_178452.4:c.*1795_*1807del (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.84213242_84213254del
DNA change (hg38) g.84179636_84179648del
Published as TAF1C(NM_001243156.1):c.1830_1842del (p.?)
ISCN -
DB-ID TAF1C_000002
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAF1C NM_005679.3 ?/. - c.1908_1920del r.(?) p.(Cys636Ter)
DNAAF1 NM_178452.4 ?/. - c.*1795_*1807del r.(=) p.(=)


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