21-43658154-C-T

Position:

• chr21-43658154-C-T

Variant summary

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

The NM_007031.2(HSF2BP):​c.-58G>A variant causes a 5 prime UTR change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.577 in 1,469,810 control chromosomes in the GnomAD database, including 247,111 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 0.58 (26390 hom., cov: 35)
  • Exomes 𝑓: 0.58 (220721 hom.)
• Consequence: HSF2BP NM_007031.2 5_prime_UTR
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.126

Genes affected

HSF2BP (HGNC:5226): (heat shock transcription factor 2 binding protein) HSF2 binding protein (HSF2BP) associates with HSF2. The interaction occurs between the trimerization domain of HSF2 and the amino terminal hydrophilic region of HSF2BP that comprises two leucine zipper motifs. HSF2BP may therefore be involved in modulating HSF2 activation. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.81).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.764 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
HSF2BP	NM_007031.2	c.-58G>A		5_prime_UTR_variant	2/9	ENST00000291560.7	NP_008962.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
HSF2BP	ENST00000291560.7	c.-58G>A		5_prime_UTR_variant	2/9	1	NM_007031.2	ENSP00000291560	P1
HSF2BP	ENST00000443485.1	c.-58G>A		5_prime_UTR_variant	2/7	5		ENSP00000409585

Frequencies

GnomAD3 genomes AF: 0.584 AC: 88817 AN: 152068 Hom.: 26359 Cov.: 35

Gnomad AFR AF: 0.522

Gnomad AMI AF: 0.562

Gnomad AMR AF: 0.675

Gnomad ASJ AF: 0.609

Gnomad EAS AF: 0.784

Gnomad SAS AF: 0.669

Gnomad FIN AF: 0.664

Gnomad MID AF: 0.623

Gnomad NFE AF: 0.567

Gnomad OTH AF: 0.578

GnomAD4 exome AF: 0.576 AC: 758625 AN: 1317624 Hom.: 220721 Cov.: 30 AF XY: 0.577 AC XY: 371958 AN XY: 644162

Gnomad4 AFR exome AF: 0.520

Gnomad4 AMR exome AF: 0.728

Gnomad4 ASJ exome AF: 0.613

Gnomad4 EAS exome AF: 0.780

Gnomad4 SAS exome AF: 0.652

Gnomad4 FIN exome AF: 0.662

Gnomad4 NFE exome AF: 0.558

Gnomad4 OTH exome AF: 0.586

GnomAD4 genome AF: 0.584 AC: 88904 AN: 152186 Hom.: 26390 Cov.: 35 AF XY: 0.595 AC XY: 44298 AN XY: 74422

Gnomad4 AFR AF: 0.522

Gnomad4 AMR AF: 0.676

Gnomad4 ASJ AF: 0.609

Gnomad4 EAS AF: 0.784

Gnomad4 SAS AF: 0.668

Gnomad4 FIN AF: 0.664

Gnomad4 NFE AF: 0.567

Gnomad4 OTH AF: 0.583

Alfa AF: 0.557 Hom.: 8443

Bravo AF: 0.579

Asia WGS AF: 0.731 AC: 2542 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.81
CADD	Benign	14
DANN	Benign	0.95

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: rs2838343; hg19: chr21-45078035; COSMIC: COSV52360104; COSMIC: COSV52360104;