rs4470077

chr14-55430820-A-G

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_199047.3(TBPL2):c.693-1846T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.28 in 152,166 control chromosomes in the GnomAD database, including 7,731 homozygotes. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.28 (7731 hom., cov: 32)
• Consequence: TBPL2 NM_199047.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.390

Genes affected

TBPL2 (HGNC:19841): (TATA-box binding protein like 2) Predicted to enable RNA polymerase II general transcription initiation factor activity. Predicted to be involved in DNA-templated transcription, initiation. Located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Apr 2022]

FBXO34 (HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.78).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.519 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
TBPL2	NM_199047.3	c.693-1846T>C		intron_variant		ENST00000247219.6
FBXO34	XR_007064022.1	n.2983-6096A>G		intron_variant, non_coding_transcript_variant
FBXO34	XR_007064023.1	n.2941-12007A>G		intron_variant, non_coding_transcript_variant
FBXO34	XR_007064024.1	n.2982+6736A>G		intron_variant, non_coding_transcript_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
TBPL2	ENST00000247219.6	c.693-1846T>C		intron_variant		1	NM_199047.3	P1

Frequencies

GnomAD3 genomes AF: 0.280 AC: 42506 AN: 152048 Hom.: 7709 Cov.: 32

Gnomad AFR AF: 0.525

Gnomad AMI AF: 0.311

Gnomad AMR AF: 0.188

Gnomad ASJ AF: 0.186

Gnomad EAS AF: 0.0942

Gnomad SAS AF: 0.186

Gnomad FIN AF: 0.191

Gnomad MID AF: 0.241

Gnomad NFE AF: 0.191

Gnomad OTH AF: 0.249

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

GnomAD4 genome AF: 0.280 AC: 42578 AN: 152166 Hom.: 7731 Cov.: 32 AF XY: 0.275 AC XY: 20422 AN XY: 74394

Gnomad4 AFR AF: 0.525

Gnomad4 AMR AF: 0.187

Gnomad4 ASJ AF: 0.186

Gnomad4 EAS AF: 0.0941

Gnomad4 SAS AF: 0.186

Gnomad4 FIN AF: 0.191

Gnomad4 NFE AF: 0.191

Gnomad4 OTH AF: 0.252

Alfa AF: 0.233 Hom.: 1086

Bravo AF: 0.291

Asia WGS AF: 0.184 AC: 637 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.78
Cadd	Benign	4.4
Dann	Benign	0.72

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

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

Publications

LitVar

Other links and lift over

dbSNP: rs4470077; hg19: chr14-55897538;