rs9648723

Positions:

• chr7-151698551-A-C
• chr7-151698551-A-G
• chr7-151698551-A-T

Variant summary

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

The NM_016203.4(PRKAG2):​c.467-22914T>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.315 in 151,626 control chromosomes in the GnomAD database, including 10,356 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 0.31 (10356 hom., cov: 31)
• Consequence: PRKAG2 NM_016203.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -2.17

Genes affected

PRKAG2 (HGNC:9386): (protein kinase AMP-activated non-catalytic subunit gamma 2) AMP-activated protein kinase (AMPK) is a heterotrimeric protein composed of a catalytic alpha subunit, a noncatalytic beta subunit, and a noncatalytic regulatory gamma subunit. Various forms of each of these subunits exist, encoded by different genes. AMPK is an important energy-sensing enzyme that monitors cellular energy status and functions by inactivating key enzymes involved in regulating de novo biosynthesis of fatty acid and cholesterol. This gene is a member of the AMPK gamma subunit family. Mutations in this gene have been associated with Wolff-Parkinson-White syndrome, familial hypertrophic cardiomyopathy, and glycogen storage disease of the heart. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jan 2015]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.09).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.607 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
PRKAG2	NM_016203.4	c.467-22914T>G		intron_variant		ENST00000287878.9

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
PRKAG2	ENST00000287878.9	c.467-22914T>G		intron_variant		1	NM_016203.4	P3

Frequencies

GnomAD3 genomes AF: 0.315 AC: 47663 AN: 151508 Hom.: 10333 Cov.: 31

Gnomad AFR AF: 0.614

Gnomad AMI AF: 0.121

Gnomad AMR AF: 0.337

Gnomad ASJ AF: 0.248

Gnomad EAS AF: 0.141

Gnomad SAS AF: 0.191

Gnomad FIN AF: 0.167

Gnomad MID AF: 0.263

Gnomad NFE AF: 0.179

Gnomad OTH AF: 0.307

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

GnomAD4 genome AF: 0.315 AC: 47739 AN: 151626 Hom.: 10356 Cov.: 31 AF XY: 0.313 AC XY: 23162 AN XY: 74056

Gnomad4 AFR AF: 0.614

Gnomad4 AMR AF: 0.337

Gnomad4 ASJ AF: 0.248

Gnomad4 EAS AF: 0.142

Gnomad4 SAS AF: 0.192

Gnomad4 FIN AF: 0.167

Gnomad4 NFE AF: 0.179

Gnomad4 OTH AF: 0.305

Alfa AF: 0.198 Hom.: 4866

Bravo AF: 0.339

Asia WGS AF: 0.174 AC: 606 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.1
CADD	Benign	0.37
DANN	Benign	0.16

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: rs9648723; hg19: chr7-151395637;