rs72829457

chr17-7665009-C-T

Variant summary

Our verdict is Benign. Variant got -10 ACMG points: 0P and 10B. BP4_Moderate BA1

The ENST00000413465.6(TP53):c.783-2995G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0637 in 152,108 control chromosomes in the GnomAD database, including 477 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 0.064 (477 hom., cov: 30)
• Consequence: TP53 ENST00000413465.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.437

Genes affected

TP53 (HGNC:11998): (tumor protein p53) This gene encodes a tumor suppressor protein containing transcriptional activation, DNA binding, and oligomerization domains. The encoded protein responds to diverse cellular stresses to regulate expression of target genes, thereby inducing cell cycle arrest, apoptosis, senescence, DNA repair, or changes in metabolism. Mutations in this gene are associated with a variety of human cancers, including hereditary cancers such as Li-Fraumeni syndrome. Alternative splicing of this gene and the use of alternate promoters result in multiple transcript variants and isoforms. Additional isoforms have also been shown to result from the use of alternate translation initiation codons from identical transcript variants (PMIDs: 12032546, 20937277). [provided by RefSeq, Dec 2016]

ACMG classification

Verdict is Benign. Variant got -10 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.34).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.101 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
TP53	ENST00000413465.6	c.783-2995G>A		intron_variant		1

Frequencies

GnomAD3 genomes AF: 0.0638 AC: 9694 AN: 151990 Hom.: 477 Cov.: 30

Gnomad AFR AF: 0.0195

Gnomad AMI AF: 0.105

Gnomad AMR AF: 0.0530

Gnomad ASJ AF: 0.0949

Gnomad EAS AF: 0.000192

Gnomad SAS AF: 0.00727

Gnomad FIN AF: 0.0465

Gnomad MID AF: 0.0127

Gnomad NFE AF: 0.103

Gnomad OTH AF: 0.0629

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

GnomAD4 genome AF: 0.0637 AC: 9690 AN: 152108 Hom.: 477 Cov.: 30 AF XY: 0.0593 AC XY: 4407 AN XY: 74342

Gnomad4 AFR AF: 0.0195

Gnomad4 AMR AF: 0.0530

Gnomad4 ASJ AF: 0.0949

Gnomad4 EAS AF: 0.000193

Gnomad4 SAS AF: 0.00748

Gnomad4 FIN AF: 0.0465

Gnomad4 NFE AF: 0.103

Gnomad4 OTH AF: 0.0622

Alfa AF: 0.0736 Hom.: 58

Bravo AF: 0.0642

Asia WGS AF: 0.00722 AC: 25 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.34
Cadd	Benign	14
Dann	Benign	0.85

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs72829457; hg19: chr17-7568327;