chr3-12329583-G-C

Position:

• chr3-12329583-G-C

Variant summary

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

The NM_138711.6(PPARG):​c.-9+17130G>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.273 in 151,920 control chromosomes in the GnomAD database, including 5,754 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 0.27 (5754 hom., cov: 32)
• Consequence: PPARG NM_138711.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.11

Genes affected

PPARG (HGNC:9236): (peroxisome proliferator activated receptor gamma) This gene encodes a member of the peroxisome proliferator-activated receptor (PPAR) subfamily of nuclear receptors. PPARs form heterodimers with retinoid X receptors (RXRs) and these heterodimers regulate transcription of various genes. Three subtypes of PPARs are known: PPAR-alpha, PPAR-delta, and PPAR-gamma. The protein encoded by this gene is PPAR-gamma and is a regulator of adipocyte differentiation. Additionally, PPAR-gamma has been implicated in the pathology of numerous diseases including obesity, diabetes, atherosclerosis and cancer. Alternatively spliced transcript variants that encode different isoforms have been described. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.95).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.314 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
PPARG	NM_138711.6	c.-9+17130G>C		intron_variant		ENST00000651735.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
PPARG	ENST00000651735.1	c.-9+17130G>C		intron_variant			NM_138711.6	P1

Frequencies

GnomAD3 genomes AF: 0.273 AC: 41410 AN: 151802 Hom.: 5737 Cov.: 32

Gnomad AFR AF: 0.298

Gnomad AMI AF: 0.134

Gnomad AMR AF: 0.296

Gnomad ASJ AF: 0.242

Gnomad EAS AF: 0.327

Gnomad SAS AF: 0.225

Gnomad FIN AF: 0.280

Gnomad MID AF: 0.232

Gnomad NFE AF: 0.255

Gnomad OTH AF: 0.243

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

GnomAD4 genome AF: 0.273 AC: 41467 AN: 151920 Hom.: 5754 Cov.: 32 AF XY: 0.273 AC XY: 20235 AN XY: 74242

Gnomad4 AFR AF: 0.298

Gnomad4 AMR AF: 0.297

Gnomad4 ASJ AF: 0.242

Gnomad4 EAS AF: 0.327

Gnomad4 SAS AF: 0.227

Gnomad4 FIN AF: 0.280

Gnomad4 NFE AF: 0.255

Gnomad4 OTH AF: 0.242

Alfa AF: 0.269 Hom.: 819

Bravo AF: 0.280

Asia WGS AF: 0.238 AC: 825 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.95
CADD	Benign	0.49
DANN	Benign	0.46

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs12496005; hg19: chr3-12371082;