rs7713645

Positions:

• chr5-68231498-A-C
• chr5-68231498-A-G
• chr5-68231498-A-T

Variant summary

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

The NM_181523.3(PIK3R1):​c.334+4489A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.58 in 152,034 control chromosomes in the GnomAD database, including 26,993 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 (26993 hom., cov: 33)
• Consequence: PIK3R1 NM_181523.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.39

Genes affected

PIK3R1 (HGNC:8979): (phosphoinositide-3-kinase regulatory subunit 1) Phosphatidylinositol 3-kinase phosphorylates the inositol ring of phosphatidylinositol at the 3-prime position. The enzyme comprises a 110 kD catalytic subunit and a regulatory subunit of either 85, 55, or 50 kD. This gene encodes the 85 kD regulatory subunit. Phosphatidylinositol 3-kinase plays an important role in the metabolic actions of insulin, and a mutation in this gene has been associated with insulin resistance. Alternative splicing of this gene results in four transcript variants encoding different isoforms. [provided by RefSeq, Jun 2011]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.778 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
PIK3R1	NM_181523.3	c.334+4489A>C		intron_variant		ENST00000521381.6	NP_852664.1
PIK3R1	XM_005248542.4	c.334+4489A>C		intron_variant			XP_005248599.1
PIK3R1	XM_017009585.3	c.334+4489A>C		intron_variant			XP_016865074.1
PIK3R1	XM_047417315.1	c.334+4489A>C		intron_variant			XP_047273271.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
PIK3R1	ENST00000521381.6	c.334+4489A>C		intron_variant		1	NM_181523.3	ENSP00000428056	P1

Frequencies

GnomAD3 genomes AF: 0.580 AC: 88079 AN: 151916 Hom.: 26923 Cov.: 33

Gnomad AFR AF: 0.784

Gnomad AMI AF: 0.550

Gnomad AMR AF: 0.546

Gnomad ASJ AF: 0.439

Gnomad EAS AF: 0.742

Gnomad SAS AF: 0.500

Gnomad FIN AF: 0.447

Gnomad MID AF: 0.427

Gnomad NFE AF: 0.487

Gnomad OTH AF: 0.531

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

GnomAD4 genome AF: 0.580 AC: 88206 AN: 152034 Hom.: 26993 Cov.: 33 AF XY: 0.577 AC XY: 42854 AN XY: 74308

Gnomad4 AFR AF: 0.785

Gnomad4 AMR AF: 0.546

Gnomad4 ASJ AF: 0.439

Gnomad4 EAS AF: 0.742

Gnomad4 SAS AF: 0.499

Gnomad4 FIN AF: 0.447

Gnomad4 NFE AF: 0.487

Gnomad4 OTH AF: 0.536

Alfa AF: 0.495 Hom.: 23946

Bravo AF: 0.601

Asia WGS AF: 0.638 AC: 2217 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	2.4
DANN	Benign	0.74

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: rs7713645; hg19: chr5-67527326; COSMIC: COSV57126721; COSMIC: COSV57126721;