rs565186

Positions:

• chr11-101112898-T-C

Variant summary

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

The NM_000926.4(PGR):​c.1789+13109A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.117 in 152,238 control chromosomes in the GnomAD database, including 1,355 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 0.12 (1355 hom., cov: 32)
• Consequence: PGR NM_000926.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.18

Genes affected

PGR (HGNC:8910): (progesterone receptor) This gene encodes a member of the steroid receptor superfamily. The encoded protein mediates the physiological effects of progesterone, which plays a central role in reproductive events associated with the establishment and maintenance of pregnancy. This gene uses two distinct promotors and translation start sites in the first exon to produce several transcript variants, both protein coding and non-protein coding. Two of the isoforms (A and B) are identical except for an additional 165 amino acids found in the N-terminus of isoform B and mediate their own response genes and physiologic effects with little overlap. [provided by RefSeq, Sep 2015]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.89).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.158 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
PGR	NM_000926.4	c.1789+13109A>G		intron_variant		ENST00000325455.10

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
PGR	ENST00000325455.10	c.1789+13109A>G		intron_variant		1	NM_000926.4	P1

Frequencies

GnomAD3 genomes AF: 0.117 AC: 17824 AN: 152120 Hom.: 1356 Cov.: 32

Gnomad AFR AF: 0.0303

Gnomad AMI AF: 0.254

Gnomad AMR AF: 0.137

Gnomad ASJ AF: 0.250

Gnomad EAS AF: 0.0117

Gnomad SAS AF: 0.0796

Gnomad FIN AF: 0.157

Gnomad MID AF: 0.137

Gnomad NFE AF: 0.161

Gnomad OTH AF: 0.134

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

GnomAD4 genome AF: 0.117 AC: 17823 AN: 152238 Hom.: 1355 Cov.: 32 AF XY: 0.115 AC XY: 8575 AN XY: 74438

Gnomad4 AFR AF: 0.0302

Gnomad4 AMR AF: 0.137

Gnomad4 ASJ AF: 0.250

Gnomad4 EAS AF: 0.0118

Gnomad4 SAS AF: 0.0793

Gnomad4 FIN AF: 0.157

Gnomad4 NFE AF: 0.161

Gnomad4 OTH AF: 0.134

Alfa AF: 0.149 Hom.: 250

Bravo AF: 0.112

Asia WGS AF: 0.0580 AC: 204 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.89
CADD	Benign	1.2
DANN	Benign	0.78

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: rs565186; hg19: chr11-100983629;