Variant #0000950745 (NC_000016.9:g.84216015G>A, NM_178452.4:c.*4568G>A (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.84216015G>A
DNA change (hg38) -
Published as TAF1C(NM_001243156.1):c.514C>T (p.(Arg172Cys)), TAF1C(NM_005679.4):c.514C>T (p.R172C)
ISCN -
DB-ID DNAAF1_000060 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) 0.0002 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +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.514C>T r.(?) p.(Arg172Cys)
DNAAF1 NM_178452.4 ?/. - c.*4568G>A r.(=) p.(=)


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