rs202066215

Variant names:

• chr18-62157777-T-A
• rs202066215
• NM_176787.5:c.253A>T

Your query was ambiguous. Multiple possible variants found:

• chr18-62157777-T-A
• chr18-62157777-T-C

Variant summary

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

The NM_176787.5(PIGN):​c.253A>T​(p.Ile85Leu) 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. 16/21 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar. Another variant affecting the same amino acid position, but resulting in a different missense (i.e. I85V) has been classified as Likely benign.

• Frequency: Genomes: not found (cov: 33)
• Consequence: PIGN NM_176787.5 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.139

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 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=0.19151413).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
PIGN	NM_176787.5	c.253A>T	p.Ile85Leu	missense_variant	Exon 5 of 31	ENST00000640252.2	NP_789744.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
PIGN	ENST00000640252.2	c.253A>T	p.Ile85Leu	missense_variant	Exon 5 of 31	1	NM_176787.5	ENSP00000492233.1
PIGN	ENST00000400334.7	c.253A>T	p.Ile85Leu	missense_variant	Exon 4 of 30	1		ENSP00000383188.2
PIGN	ENST00000638424.1	n.253A>T		non_coding_transcript_exon_variant	Exon 3 of 29	5		ENSP00000491963.1

Frequencies

GnomAD3 genomes Cov.: 33

GnomAD4 exome Cov.: 30

GnomAD4 genome Cov.: 33

ExAC AF: 0.00000827 AC: 1

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.14
BayesDel_addAF	Benign	-0.10	T
BayesDel_noAF	Benign	-0.38
CADD	Benign	4.9
DANN	Benign	0.89
DEOGEN2	Benign	0.047	T;.;T;T;T;.;.;.;.;.;T;.;.;T;.;T;.;.;.;.;.;.;.;.;.;T;T;T;.
Eigen	Benign	-1.3
Eigen_PC	Benign	-1.4
FATHMM_MKL	Benign	0.19	N
LIST_S2	Benign	0.84	.;.;.;.;.;.;T;.;T;T;.;T;T;.;T;T;T;T;.;.;T;T;T;T;T;.;T;T;T
M_CAP	Benign	0.044	D
MetaRNN	Benign	0.19	T;T;T;T;T;T;T;T;T;T;T;T;T;T;T;T;T;T;T;T;T;T;T;T;T;T;T;T;T
MetaSVM	Benign	-0.83	T
MutationAssessor	Benign	2.0	M;.;M;M;M;.;.;.;.;.;M;.;.;M;.;M;.;.;.;.;.;.;.;.;.;.;.;.;.
PrimateAI	Benign	0.31	T
PROVEAN	Benign	-1.9	.;.;.;N;.;.;.;.;.;.;N;.;.;.;.;.;.;.;.;.;.;.;.;.;.;.;.;.;.
REVEL	Benign	0.15
Sift	Uncertain	0.013	.;.;.;D;.;.;.;.;.;.;D;.;.;.;.;.;.;.;.;.;.;.;.;.;.;.;.;.;.
Sift4G	Benign	0.14	.;.;.;T;.;.;.;.;.;.;T;.;.;.;.;.;.;.;.;.;.;.;.;.;.;.;.;T;.
Polyphen		0.0090	B;.;B;B;B;.;.;.;.;.;B;.;.;B;.;B;.;.;.;.;.;.;.;.;.;.;.;.;.
Vest4		0.29, 0.29
MutPred		0.63		Gain of disorder (P = 0.1458);Gain of disorder (P = 0.1458);Gain of disorder (P = 0.1458);Gain of disorder (P = 0.1458);Gain of disorder (P = 0.1458);Gain of disorder (P = 0.1458);Gain of disorder (P = 0.1458);Gain of disorder (P = 0.1458);Gain of disorder (P = 0.1458);.;Gain of disorder (P = 0.1458);Gain of disorder (P = 0.1458);Gain of disorder (P = 0.1458);Gain of disorder (P = 0.1458);Gain of disorder (P = 0.1458);Gain of disorder (P = 0.1458);Gain of disorder (P = 0.1458);Gain of disorder (P = 0.1458);Gain of disorder (P = 0.1458);Gain of disorder (P = 0.1458);Gain of disorder (P = 0.1458);Gain of disorder (P = 0.1458);Gain of disorder (P = 0.1458);Gain of disorder (P = 0.1458);Gain of disorder (P = 0.1458);Gain of disorder (P = 0.1458);Gain of disorder (P = 0.1458);.;Gain of disorder (P = 0.1458);
MVP		0.58
MPC		0.024
ClinPred		0.12	T
GERP RS		-4.9
Varity_R		0.12
gMVP		0.61

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.010		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: rs202066215; hg19: chr18-59825010;