rs13381627

Positions:

• chr18-62114567-A-C
• chr18-62114567-A-G

Variant summary

Our verdict is Likely benign. Variant got -2 ACMG points: 2P and 4B. PM2 BP4_Strong

The NM_176787.5(PIGN):​c.1245T>G​(p.Asp415Glu) 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. D415D) has been classified as Benign.

• Frequency: Genomes: not found (cov: 31)
• Consequence: PIGN NM_176787.5 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.567

Genes affected

PIGN (HGNC:8967): (phosphatidylinositol glycan anchor biosynthesis class N) This gene encodes a protein that is involved in glycosylphosphatidylinositol (GPI)-anchor biosynthesis. The GPI-anchor is a glycolipid found on many blood cells and serves to anchor proteins to the cell surface. This protein is expressed in the endoplasmic reticulum and transfers phosphoethanolamine (EtNP) to the first mannose of the GPI anchor. Two alternatively spliced variants, which encode an identical isoform, have been reported. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Likely_benign. Variant got -2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.04461059).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
PIGN	NM_176787.5	c.1245T>G	p.Asp415Glu	missense_variant	15/31	ENST00000640252.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
PIGN	ENST00000640252.2	c.1245T>G	p.Asp415Glu	missense_variant	15/31	1	NM_176787.5	P1

Frequencies

GnomAD3 genomes Cov.: 31

GnomAD4 exome Cov.: 24

GnomAD4 genome Cov.: 31

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.083
BayesDel_addAF	Benign	-0.38	T
BayesDel_noAF	Benign	-0.79
CADD	Benign	0.026
DANN	Benign	0.31
DEOGEN2	Benign	0.010	T;.;T;T;T;.;.;.;.;T;.;.;T;.;T;.;.;.;.;.
Eigen	Benign	-1.5
Eigen_PC	Benign	-1.4
FATHMM_MKL	Benign	0.18	N
LIST_S2	Benign	0.65	.;.;.;.;.;.;.;T;T;.;T;T;.;T;T;T;T;.;.;T
M_CAP	Benign	0.0051	T
MetaRNN	Benign	0.045	T;T;T;T;T;T;T;T;T;T;T;T;T;T;T;T;T;T;T;T
MetaSVM	Benign	-0.98	T
MutationAssessor	Benign	0.47	N;.;N;N;N;.;.;.;.;N;.;.;N;.;N;.;.;.;.;.
MutationTaster	Benign	0.94	P;P
PrimateAI	Benign	0.32	T
PROVEAN	Benign	0.11	.;.;.;N;.;.;.;.;.;N;.;.;.;.;.;.;.;.;.;.
REVEL	Benign	0.028
Sift	Benign	0.51	.;.;.;T;.;.;.;.;.;T;.;.;.;.;.;.;.;.;.;.
Sift4G	Benign	0.90	.;.;.;T;.;.;.;.;.;T;.;.;.;.;.;.;.;.;.;.
Polyphen		0.0010	B;.;B;B;B;.;.;.;.;B;.;.;B;.;B;.;.;.;.;.
Vest4		0.054, 0.053
MutPred		0.26		Loss of MoRF binding (P = 0.0791);.;Loss of MoRF binding (P = 0.0791);Loss of MoRF binding (P = 0.0791);Loss of MoRF binding (P = 0.0791);.;Loss of MoRF binding (P = 0.0791);.;.;Loss of MoRF binding (P = 0.0791);Loss of MoRF binding (P = 0.0791);.;Loss of MoRF binding (P = 0.0791);Loss of MoRF binding (P = 0.0791);Loss of MoRF binding (P = 0.0791);Loss of MoRF binding (P = 0.0791);Loss of MoRF binding (P = 0.0791);Loss of MoRF binding (P = 0.0791);Loss of MoRF binding (P = 0.0791);Loss of MoRF binding (P = 0.0791);
MVP		0.31
MPC		0.023
ClinPred		0.023	T
GERP RS		-2.8
Varity_R		0.036
gMVP		0.075

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.050		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: rs13381627; hg19: chr18-59781800;