rs13095453

chr3-141356120-G-A

Variant summary

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

The ENST00000509842.5(ZBTB38):c.-738-12501G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.264 in 151,932 control chromosomes in the GnomAD database, including 5,902 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 0.26 (5902 hom., cov: 32)
• Consequence: ZBTB38 ENST00000509842.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.587

Genes affected

ZBTB38 (HGNC:26636): (zinc finger and BTB domain containing 38) The protein encoded by this gene is a zinc finger transcriptional activator that binds methylated DNA. The encoded protein can form homodimers or heterodimers through the zinc finger domains. In mouse, inhibition of this protein has been associated with apoptosis in some cell types. [provided by RefSeq, Jun 2010]

(HGNC:):

PXYLP1 (HGNC:26303): (2-phosphoxylose phosphatase 1) Enables phosphatase activity. Involved in chondroitin sulfate proteoglycan biosynthetic process; glycosaminoglycan biosynthetic process; and positive regulation of heparan sulfate proteoglycan biosynthetic process. Located in Golgi apparatus. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.86).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.316 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
ZBTB38	NM_001080412.3	c.-738-12501G>A		intron_variant
ZBTB38	XM_047447849.1	c.-566-12501G>A		intron_variant
ZBTB38	XM_047447855.1	c.-493-12501G>A		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
ZBTB38	ENST00000509842.5	c.-738-12501G>A		intron_variant		1
	ENST00000507698.1	n.166+10181C>T		intron_variant, non_coding_transcript_variant		3
PXYLP1	ENST00000637579.1	c.*290-10126G>A		intron_variant, NMD_transcript_variant		5

Frequencies

GnomAD3 genomes AF: 0.264 AC: 40101 AN: 151814 Hom.: 5903 Cov.: 32

Gnomad AFR AF: 0.216

Gnomad AMI AF: 0.267

Gnomad AMR AF: 0.178

Gnomad ASJ AF: 0.301

Gnomad EAS AF: 0.00212

Gnomad SAS AF: 0.176

Gnomad FIN AF: 0.385

Gnomad MID AF: 0.261

Gnomad NFE AF: 0.319

Gnomad OTH AF: 0.230

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

GnomAD4 genome AF: 0.264 AC: 40106 AN: 151932 Hom.: 5902 Cov.: 32 AF XY: 0.260 AC XY: 19336 AN XY: 74258

Gnomad4 AFR AF: 0.216

Gnomad4 AMR AF: 0.178

Gnomad4 ASJ AF: 0.301

Gnomad4 EAS AF: 0.00213

Gnomad4 SAS AF: 0.177

Gnomad4 FIN AF: 0.385

Gnomad4 NFE AF: 0.319

Gnomad4 OTH AF: 0.227

Alfa AF: 0.295 Hom.: 11927

Bravo AF: 0.246

Asia WGS AF: 0.0880 AC: 307 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.86
Cadd	Benign	2.6
Dann	Benign	0.61

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs13095453; hg19: chr3-141074962;