rs41481947

Variant names:

• chrX-71431003-ATTTTTTTTTTTTTTTTTT-A
• rs41481947
• NM_004606.5:c.4753+6777_4753+6794delTTTTTTTTTTTTTTTTTT

Your query was ambiguous. Multiple possible variants found:

• chrX-71431003-ATTTTTTTTTTTTTTTTTT-A
• chrX-71431003-ATTTTTTTTTTTTTTTTTT-ATT
• chrX-71431003-ATTTTTTTTTTTTTTTTTT-ATTTT
• chrX-71431003-ATTTTTTTTTTTTTTTTTT-ATTTTT
• chrX-71431003-ATTTTTTTTTTTTTTTTTT-ATTTTTT
• chrX-71431003-ATTTTTTTTTTTTTTTTTT-ATTTTTTT
• chrX-71431003-ATTTTTTTTTTTTTTTTTT-ATTTTTTTT
• chrX-71431003-ATTTTTTTTTTTTTTTTTT-ATTTTTTTTT
• chrX-71431003-ATTTTTTTTTTTTTTTTTT-ATTTTTTTTTT
• chrX-71431003-ATTTTTTTTTTTTTTTTTT-ATTTTTTTTTTT
• chrX-71431003-ATTTTTTTTTTTTTTTTTT-ATTTTTTTTTTTT
• chrX-71431003-ATTTTTTTTTTTTTTTTTT-ATTTTTTTTTTTTT
• chrX-71431003-ATTTTTTTTTTTTTTTTTT-ATTTTTTTTTTTTTT
• chrX-71431003-ATTTTTTTTTTTTTTTTTT-ATTTTTTTTTTTTTTT
• chrX-71431003-ATTTTTTTTTTTTTTTTTT-ATTTTTTTTTTTTTTTT
• chrX-71431003-ATTTTTTTTTTTTTTTTTT-ATTTTTTTTTTTTTTTTT
• chrX-71431003-ATTTTTTTTTTTTTTTTTT-ATTTTTTTTTTTTTTTTTTT
• chrX-71431003-ATTTTTTTTTTTTTTTTTT-ATTTTTTTTTTTTTTTTTTTT
• chrX-71431003-ATTTTTTTTTTTTTTTTTT-ATTTTTTTTTTTTTTTTTTTTT
• chrX-71431003-ATTTTTTTTTTTTTTTTTT-ATTTTTTTTTTTTTTTTTTTTTT
• chrX-71431003-ATTTTTTTTTTTTTTTTTT-ATTTTTTTTTTTTTTTTTTTTTTT
• chrX-71431003-ATTTTTTTTTTTTTTTTTT-ATTTTTTTTTTTTTTTTTTTTTTTT
• chrX-71431003-ATTTTTTTTTTTTTTTTTT-ATTTTTTTTTTTTTTTTTTTTTTTTT
• chrX-71431003-ATTTTTTTTTTTTTTTTTT-ATTTTTTTTTTTTTTTTTTTTTTTTTT
• chrX-71431003-ATTTTTTTTTTTTTTTTTT-ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Variant summary

Our verdict is Uncertain significance. The variant received 0 ACMG points: 0P and 0B.

The NM_004606.5(TAF1):​c.4753+6777_4753+6794delTTTTTTTTTTTTTTTTTT variant causes a intron change involving the alteration of a non-conserved nucleotide. It is difficult to determine the true allele frequency of this variant because it is of type DEL_BIG, and the frequency of such variant types in population databases may be underestimated and unreliable. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: not found (cov: 15)
• Consequence: TAF1 NM_004606.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.646
• Publications: 0 publications found

Genes affected

TAF1 (HGNC:11535): (TATA-box binding protein associated factor 1) Initiation of transcription by RNA polymerase II requires the activities of more than 70 polypeptides. The protein that coordinates these activities is the basal transcription factor TFIID, which binds to the core promoter to position the polymerase properly, serves as the scaffold for assembly of the remainder of the transcription complex, and acts as a channel for regulatory signals. TFIID is composed of the TATA-binding protein (TBP) and a group of evolutionarily conserved proteins known as TBP-associated factors or TAFs. TAFs may participate in basal transcription, serve as coactivators, function in promoter recognition or modify general transcription factors (GTFs) to facilitate complex assembly and transcription initiation. This gene encodes the largest subunit of TFIID. This subunit binds to core promoter sequences encompassing the transcription start site. It also binds to activators and other transcriptional regulators, and these interactions affect the rate of transcription initiation. This subunit contains two independent protein kinase domains at the N- and C-terminals, but also possesses acetyltransferase activity and can act as a ubiquitin-activating/conjugating enzyme. Mutations in this gene result in Dystonia 3, torsion, X-linked, a dystonia-parkinsonism disorder. Alternative splicing of this gene results in multiple transcript variants. This gene is part of a complex transcription unit (TAF1/DYT3), wherein some transcript variants share exons with TAF1 as well as additional downstream DYT3 exons. [provided by RefSeq, Oct 2013]

TAF1 Gene-Disease associations (from GenCC):

• intellectual disability, X-linked, syndromic 33

  Inheritance: XL Classification: DEFINITIVE, STRONG Submitted by: Ambry Genetics, Labcorp Genetics (formerly Invitae), G2P, Illumina
• X-linked dystonia-parkinsonism

  Inheritance: XL, Unknown Classification: STRONG, MODERATE, SUPPORTIVE, LIMITED Submitted by: Ambry Genetics, Genomics England PanelApp, Orphanet, Labcorp Genetics (formerly Invitae)
• X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome

  Inheritance: XL Classification: SUPPORTIVE Submitted by: Orphanet

ACMG classification

Our verdict: Uncertain_significance. The variant received 0 ACMG points.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
TAF1	NM_004606.5	c.4753+6777_4753+6794delTTTTTTTTTTTTTTTTTT		intron_variant	Intron 32 of 37	ENST00000423759.6	NP_004597.3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
TAF1	ENST00000423759.6	c.4753+6766_4753+6783delTTTTTTTTTTTTTTTTTT		intron_variant	Intron 32 of 37	5	NM_004606.5	ENSP00000406549.2

Frequencies

GnomAD3 genomes Cov.: 15

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome Cov.: 15

Alfa AF: 0.00 Hom.: 26

Bravo AF: 0.00000378

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
PhyloP100		0.65

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs41481947; hg19: chrX-70650853;