ENST00000555220.5:c.174-14276T>C

Variant names:

• chr14-64463914-A-G
• rs745686
• ENST00000555220.5:c.174-14276T>C

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The ENST00000555220.5(ZBTB25):​c.174-14276T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.341 in 152,110 control chromosomes in the GnomAD database, including 8,979 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 0.34 (8979 hom., cov: 32)
• Consequence: ZBTB25 ENST00000555220.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0750
• Publications: 28 publications found

Genes affected

ZBTB25 (HGNC:13112): (zinc finger and BTB domain containing 25) Predicted to enable DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.88).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.562 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000555220.5. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ZBTB25	NM_001304508.1		c.174-14276T>C		intron	N/A	NP_001291437.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ZBTB25	ENST00000555220.5	TSL:1	c.174-14276T>C		intron	N/A	ENSP00000450718.1
	ZBTB25	ENST00000555424.1	TSL:5	c.257-14276T>C		intron	N/A	ENSP00000451046.1

Frequencies

GnomAD3 genomes AF: 0.341 AC: 51897 AN: 151992 Hom.: 8979 Cov.: 32

Gnomad AFR AF: 0.319

Gnomad AMI AF: 0.277

Gnomad AMR AF: 0.310

Gnomad ASJ AF: 0.315

Gnomad EAS AF: 0.580

Gnomad SAS AF: 0.283

Gnomad FIN AF: 0.404

Gnomad MID AF: 0.304

Gnomad NFE AF: 0.340

Gnomad OTH AF: 0.338

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

GnomAD4 genome AF: 0.341 AC: 51923 AN: 152110 Hom.: 8979 Cov.: 32 AF XY: 0.345 AC XY: 25642 AN XY: 74324

African (AFR) AF: 0.319 AC: 13244 AN: 41484

American (AMR) AF: 0.310 AC: 4739 AN: 15266

Ashkenazi Jewish (ASJ) AF: 0.315 AC: 1095 AN: 3472

East Asian (EAS) AF: 0.580 AC: 3003 AN: 5182

South Asian (SAS) AF: 0.284 AC: 1371 AN: 4822

European-Finnish (FIN) AF: 0.404 AC: 4265 AN: 10558

Middle Eastern (MID) AF: 0.299 AC: 88 AN: 294

European-Non Finnish (NFE) AF: 0.340 AC: 23150 AN: 68010

Other (OTH) AF: 0.339 AC: 716 AN: 2112

Alfa AF: 0.340 Hom.: 28632

Bravo AF: 0.337

Asia WGS AF: 0.418 AC: 1451 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.88
CADD	Benign	3.5
DANN	Benign	0.49
PhyloP100		0.075
Mutation Taster		=100/0	polymorphism (auto)

Splicing

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

Other links and lift over

dbSNP: rs745686; hg19: chr14-64930632;