rs7259175

Variant names:

• chr19-52223795-C-T
• rs7259175
• NM_014225.6:c.1661+1554C>T

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_014225.6(PPP2R1A):​c.1661+1554C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.156 in 152,034 control chromosomes in the GnomAD database, including 2,310 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 0.16 (2310 hom., cov: 32)
• Consequence: PPP2R1A NM_014225.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.386
• Publications: 2 publications found

Genes affected

PPP2R1A (HGNC:9302): (protein phosphatase 2 scaffold subunit Aalpha) This gene encodes a constant regulatory subunit of protein phosphatase 2. Protein phosphatase 2 is one of the four major Ser/Thr phosphatases, and it is implicated in the negative control of cell growth and division. It consists of a common heteromeric core enzyme, which is composed of a catalytic subunit and a constant regulatory subunit, that associates with a variety of regulatory subunits. The constant regulatory subunit A serves as a scaffolding molecule to coordinate the assembly of the catalytic subunit and a variable regulatory B subunit. This gene encodes an alpha isoform of the constant regulatory subunit A. Alternatively spliced transcript variants have been described. [provided by RefSeq, Apr 2010]

PPP2R1A Gene-Disease associations (from GenCC):

• complex neurodevelopmental disorder

  Inheritance: AD Classification: DEFINITIVE Submitted by: ClinGen
• Houge-Janssens syndrome 2

  Inheritance: AD Classification: DEFINITIVE, STRONG, SUPPORTIVE Submitted by: Illumina, Orphanet, Labcorp Genetics (formerly Invitae), G2P

PPP2R1A-AS1 (HGNC:58324):

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.89).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.276 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_014225.6. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	PPP2R1A	NM_014225.6	MANE Select	c.1661+1554C>T		intron	N/A	NP_055040.2
	PPP2R1A	NM_001363656.2		c.1124+1554C>T		intron	N/A	NP_001350585.1	B3KQV6
	PPP2R1A	NR_033500.2		n.1605+1554C>T		intron	N/A

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	PPP2R1A	ENST00000322088.11	TSL:1 MANE Select	c.1661+1554C>T		intron	N/A	ENSP00000324804.6	P30153
	PPP2R1A	ENST00000454220.7	TSL:1	c.1781+1554C>T		intron	N/A	ENSP00000391905.3	C9J9C1
	PPP2R1A	ENST00000703398.1		c.1703+1554C>T		intron	N/A	ENSP00000515288.1	A0A994J3H1

Frequencies

GnomAD3 genomes AF: 0.155 AC: 23620 AN: 151916 Hom.: 2306 Cov.: 32

Gnomad AFR AF: 0.280

Gnomad AMI AF: 0.0537

Gnomad AMR AF: 0.0893

Gnomad ASJ AF: 0.0758

Gnomad EAS AF: 0.0942

Gnomad SAS AF: 0.0661

Gnomad FIN AF: 0.138

Gnomad MID AF: 0.0823

Gnomad NFE AF: 0.115

Gnomad OTH AF: 0.120

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

GnomAD4 genome AF: 0.156 AC: 23658 AN: 152034 Hom.: 2310 Cov.: 32 AF XY: 0.153 AC XY: 11358 AN XY: 74318

African (AFR) AF: 0.280 AC: 11592 AN: 41424

American (AMR) AF: 0.0892 AC: 1364 AN: 15290

Ashkenazi Jewish (ASJ) AF: 0.0758 AC: 263 AN: 3470

East Asian (EAS) AF: 0.0944 AC: 487 AN: 5158

South Asian (SAS) AF: 0.0649 AC: 313 AN: 4824

European-Finnish (FIN) AF: 0.138 AC: 1458 AN: 10570

Middle Eastern (MID) AF: 0.0952 AC: 28 AN: 294

European-Non Finnish (NFE) AF: 0.115 AC: 7849 AN: 67980

Other (OTH) AF: 0.121 AC: 255 AN: 2112

Alfa AF: 0.124 Hom.: 5728

Bravo AF: 0.158

Asia WGS AF: 0.106 AC: 368 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.89
CADD	Benign	3.9
DANN	Benign	0.75
PhyloP100		-0.39
Mutation Taster		=100/0	polymorphism (auto)

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

Other links and lift over

dbSNP: rs7259175; hg19: chr19-52727048;