NM_000266.4:c.131A>G

Variant names:

• chrX-43958515-T-C
• rs104894870
• NM_000266.4:c.131A>G

Variant summary

Our verdict is Likely pathogenic. Variant got 8 ACMG points: 8P and 0B. PM1 PM2 PP3_Moderate PP5_Moderate

The NM_000266.4(NDP):​c.131A>G​(p.Tyr44Cys) variant causes a missense change. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a pathogenic outcome for this variant. Variant has been reported in ClinVar as Likely pathogenic (★).

• Frequency: Genomes: not found (cov: 23)
• Consequence: NDP NM_000266.4 missense
• Clinical Significance: Likely pathogenic criteria provided, single submitter P:2
• Conservation: PhyloP100: 4.73

Genes affected

NDP (HGNC:7678): (norrin cystine knot growth factor NDP) This gene encodes a secreted protein with a cystein-knot motif that activates the Wnt/beta-catenin pathway. The protein forms disulfide-linked oligomers in the extracellular matrix. Mutations in this gene result in Norrie disease and X-linked exudative vitreoretinopathy. [provided by RefSeq, Feb 2009]

NDP-AS1 (HGNC:40395): (NDP antisense RNA 1)

ACMG classification

Verdict is Likely_pathogenic. Variant got 8 ACMG points.

• PM1: In a hotspot region, there are 5 aminoacids with missense pathogenic changes in the window of +-8 aminoacids around while only 0 benign, 7 uncertain in NM_000266.4
• PM2: Very rare variant in population databases, with high coverage
• PP3: MetaRNN computational evidence supports a deleterious effect, 0.903
• PP5: Variant X-43958515-T-C is Pathogenic according to our data. Variant chrX-43958515-T-C is described in ClinVar as [Likely_pathogenic]. Clinvar id is 10682.Status of the report is criteria_provided_single_submitter, 1 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
NDP	NM_000266.4	c.131A>G	p.Tyr44Cys	missense_variant	Exon 2 of 3	ENST00000642620.1	NP_000257.1
NDP-AS1	NR_046631.1	n.467-2270T>C		intron_variant	Intron 3 of 5

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
NDP	ENST00000642620.1	c.131A>G	p.Tyr44Cys	missense_variant	Exon 2 of 3		NM_000266.4	ENSP00000495972.1
NDP	ENST00000647044.1	c.131A>G	p.Tyr44Cys	missense_variant	Exon 3 of 4			ENSP00000495811.1
NDP-AS1	ENST00000435093.1	n.467-2270T>C		intron_variant	Intron 3 of 4	3
NDP	ENST00000470584.1	n.218+203A>G		intron_variant	Intron 2 of 2	2

Frequencies

GnomAD3 genomes Cov.: 23

GnomAD4 exome Cov.: 30

GnomAD4 genome Cov.: 23

Alfa AF: 0.00209 Hom.: 0

ClinVar

Significance: Likely pathogenic

Submissions summary: Pathogenic:2

Revision: criteria provided, single submitter

Submissions by phenotype

not provided Pathogenic:1

Jul 03, 2023

Labcorp Genetics (formerly Invitae), Labcorp

Significance: Likely pathogenic

Review Status: criteria provided, single submitter

Collection Method: clinical testing

This sequence change replaces tyrosine, which is neutral and polar, with cysteine, which is neutral and slightly polar, at codon 44 of the NDP protein (p.Tyr44Cys). In summary, the currently available evidence indicates that the variant is pathogenic, but additional data are needed to prove that conclusively. Therefore, this variant has been classified as Likely Pathogenic. Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) has been performed at Invitae for this missense variant, however the output from this modeling did not meet the statistical confidence thresholds required to predict the impact of this variant on NDP protein function. ClinVar contains an entry for this variant (Variation ID: 10682). This missense change has been observed in individual(s) with exudative vitreoretinopathy and/or Norrie disease (PMID: 1303264, 14635119; Invitae). This variant is not present in population databases (gnomAD no frequency). -

Atrophia bulborum hereditaria Pathogenic:1

Oct 01, 1992

OMIM

Significance: Pathogenic

Review Status: no assertion criteria provided

Collection Method: literature only

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Pathogenic	0.98
BayesDel_addAF	Pathogenic	0.60	D
BayesDel_noAF	Pathogenic	0.62
CADD	Pathogenic	26
DANN	Uncertain	1.0
DEOGEN2	Benign	0.35	T;T;T
FATHMM_MKL	Uncertain	0.91	D
LIST_S2	Uncertain	0.95	.;.;D
M_CAP	Pathogenic	0.61	D
MetaRNN	Pathogenic	0.90	D;D;D
MetaSVM	Pathogenic	1.1	D
MutationAssessor	Benign	0.81	L;L;L
PrimateAI	Pathogenic	0.80	T
PROVEAN	Benign	2.9	.;N;.
REVEL	Pathogenic	0.69
Sift	Uncertain	0.0010	.;D;.
Sift4G	Uncertain	0.0040	.;D;.
Polyphen		1.0	D;D;D
Vest4		0.66
MutPred		0.74		Loss of sheet (P = 0.0457);Loss of sheet (P = 0.0457);Loss of sheet (P = 0.0457);
MVP		1.0
MPC		1.6
ClinPred		0.74	D
GERP RS		6.0
Varity_R		0.73
gMVP		0.97

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.070		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: rs104894870; hg19: chrX-43817761; COSMIC: COSV65204039;