Variant #0001044484 (NC_000023.10:g.70597631C>G, NM_004606.3:c.953C>G (TAF1))

Chromosome X
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.70597631C>G
DNA change (hg38) -
Published as TAF1(NM_001286074.2):c.893C>G (p.A298G), TAF1(NM_004606.5):c.893C>G (p.(Ala298Gly))
ISCN -
DB-ID TAF1_000036 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) 0.00322 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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAF1 NM_004606.3 -?/. - c.953C>G r.(?) p.(Ala318Gly)


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