rs6759

chr1-226882036-C-Achr1-226882036-C-Gchr1-226882036-C-T

Variant summary

Our verdict is Uncertain significance. Variant got 0 ACMG points: 2P and 2B. PM2 BP4_Moderate

The NM_000447.3(PSEN2):c.129C>A(p.Asn43Lys) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. 15/21 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar. Synonymous variant affecting the same amino acid position (i.e. N43N) has been classified as Benign.

• Frequency: Genomes: not found (cov: 33)
• Consequence: PSEN2 NM_000447.3 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.345

Genes affected

PSEN2 (HGNC:9509): (presenilin 2) Alzheimer's disease (AD) patients with an inherited form of the disease carry mutations in the presenilin proteins (PSEN1 or PSEN2) or the amyloid precursor protein (APP). These disease-linked mutations result in increased production of the longer form of amyloid-beta (main component of amyloid deposits found in AD brains). Presenilins are postulated to regulate APP processing through their effects on gamma-secretase, an enzyme that cleaves APP. Also, it is thought that the presenilins are involved in the cleavage of the Notch receptor such that, they either directly regulate gamma-secretase activity, or themselves act are protease enzymes. Two alternatively spliced transcript variants encoding different isoforms of PSEN2 have been identified. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Uncertain_significance. Variant got 0 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.08416468).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
PSEN2	NM_000447.3	c.129C>A	p.Asn43Lys	missense_variant	4/13	ENST00000366783.8

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
PSEN2	ENST00000366783.8	c.129C>A	p.Asn43Lys	missense_variant	4/13	5	NM_000447.3	P4

Frequencies

GnomAD3 genomes Cov.: 33

GnomAD4 exome Cov.: 66

GnomAD4 genome Cov.: 33

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.089
BayesDel_addAF	Benign	-0.027	T
BayesDel_noAF	Benign	-0.28
Cadd	Benign	1.3
Dann	Benign	0.36
DEOGEN2	Benign	0.25	T;.;.;.;.
Eigen	Benign	-1.4
Eigen_PC	Benign	-1.4
FATHMM_MKL	Benign	0.058	N
LIST_S2	Benign	0.69	T;T;T;.;T
M_CAP	Pathogenic	0.43	D
MetaRNN	Benign	0.084	T;T;T;T;T
MetaSVM	Pathogenic	1.3	D
MutationAssessor	Benign	1.0	L;.;L;.;.
MutationTaster	Benign	1.0	P;P;P;P;P
PrimateAI	Benign	0.37	T
PROVEAN	Benign	-1.2	N;N;N;N;.
REVEL	Benign	0.23
Sift	Benign	0.94	T;T;T;T;.
Sift4G	Benign	0.91	T;T;T;T;T
Polyphen		0.062	B;.;.;.;.
Vest4		0.10
MutPred		0.22		Gain of ubiquitination at N43 (P = 0.0025);Gain of ubiquitination at N43 (P = 0.0025);Gain of ubiquitination at N43 (P = 0.0025);.;.;
MVP		0.86
MPC		0.29
ClinPred		0.015	T
GERP RS		-6.8
Varity_R		0.029
gMVP		0.11

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.060		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: rs6759; hg19: chr1-227069737;