5-149826429-G-A

Position:

• chr5-149826429-G-A

Variant summary

Our verdict is Benign. Variant got -14 ACMG points: 0P and 14B. BP4_Strong BP6_Moderate BA1

The NM_133263.4(PPARGC1B):​c.253-244G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0577 in 152,208 control chromosomes in the GnomAD database, including 374 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★).

• Frequency: Genomes: 𝑓 0.058 (374 hom., cov: 33)
• Consequence: PPARGC1B NM_133263.4 intron
• Clinical Significance: Benign criteria provided, single submitter B:1
• Conservation: PhyloP100: -0.552

Genes affected

PPARGC1B (HGNC:30022): (PPARG coactivator 1 beta) The protein encoded by this gene stimulates the activity of several transcription factors and nuclear receptors, including estrogen receptor alpha, nuclear respiratory factor 1, and glucocorticoid receptor. The encoded protein may be involved in fat oxidation, non-oxidative glucose metabolism, and the regulation of energy expenditure. This protein is downregulated in prediabetic and type 2 diabetes mellitus patients. Certain allelic variations in this gene increase the risk of the development of obesity. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2010]

ACMG classification

Verdict is Benign. Variant got -14 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.93).
• BP6: Variant 5-149826429-G-A is Benign according to our data. Variant chr5-149826429-G-A is described in ClinVar as [Benign]. Clinvar id is 1221620.Status of the report is criteria_provided_single_submitter, 1 stars.
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.142 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
PPARGC1B	NM_133263.4	c.253-244G>A		intron_variant		ENST00000309241.10	NP_573570.3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
PPARGC1B	ENST00000309241.10	c.253-244G>A		intron_variant		1	NM_133263.4	ENSP00000312649	P2
PPARGC1B	ENST00000360453.8	c.253-244G>A		intron_variant		1		ENSP00000353638	A2
PPARGC1B	ENST00000394320.7	c.253-244G>A		intron_variant		1		ENSP00000377855	A2
PPARGC1B	ENST00000403750.5	c.178-244G>A		intron_variant		2		ENSP00000384403	A2

Frequencies

GnomAD3 genomes AF: 0.0576 AC: 8756 AN: 152090 Hom.: 368 Cov.: 33

Gnomad AFR AF: 0.0516

Gnomad AMI AF: 0.00987

Gnomad AMR AF: 0.146

Gnomad ASJ AF: 0.0184

Gnomad EAS AF: 0.0890

Gnomad SAS AF: 0.0384

Gnomad FIN AF: 0.0626

Gnomad MID AF: 0.0222

Gnomad NFE AF: 0.0424

Gnomad OTH AF: 0.0531

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

GnomAD4 genome AF: 0.0577 AC: 8785 AN: 152208 Hom.: 374 Cov.: 33 AF XY: 0.0592 AC XY: 4407 AN XY: 74416

Gnomad4 AFR AF: 0.0518

Gnomad4 AMR AF: 0.147

Gnomad4 ASJ AF: 0.0184

Gnomad4 EAS AF: 0.0886

Gnomad4 SAS AF: 0.0386

Gnomad4 FIN AF: 0.0626

Gnomad4 NFE AF: 0.0423

Gnomad4 OTH AF: 0.0553

Alfa AF: 0.0538 Hom.: 42

Bravo AF: 0.0693

Asia WGS AF: 0.0660 AC: 230 AN: 3478

ClinVar

Significance: Benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

Submissions by phenotype

not provided Benign:1

Benign, criteria provided, single submitter

clinical testing

GeneDx

Jun 20, 2021

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.93
CADD	Benign	0.018
DANN	Benign	0.22

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: rs741582; hg19: chr5-149205992;