rs140653237

Variant names:

• chrX-43949789-G-A
• rs140653237
• NM_000266.4:c.*10C>T

Your query was ambiguous. Multiple possible variants found:

• chrX-43949789-G-A
• chrX-43949789-G-C

Variant summary

Our verdict is Likely benign. The variant received -2 ACMG points: 2P and 4B. PM2 BP4_Strong

The NM_000266.4(NDP):​c.*10C>T variant causes a 3 prime UTR change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00000095 in 1,052,587 control chromosomes in the GnomAD database, with no homozygous occurrence. There are no hemizygote samples in GnomAD. 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: not found (cov: 22)
  • Exomes 𝑓: 9.5e-7 (0 hom. 0 hem.)
• Consequence: NDP NM_000266.4 3_prime_UTR
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0610
• Publications: 0 publications found

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

Our verdict: Likely_benign. The variant received -2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.79).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
NDP	NM_000266.4	c.*10C>T		3_prime_UTR_variant	Exon 3 of 3	ENST00000642620.1	NP_000257.1
NDP-AS1	NR_046631.1	n.58G>A		non_coding_transcript_exon_variant	Exon 1 of 6

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
NDP	ENST00000642620.1	c.*10C>T		3_prime_UTR_variant	Exon 3 of 3		NM_000266.4	ENSP00000495972.1
NDP-AS1	ENST00000435093.1	n.58G>A		non_coding_transcript_exon_variant	Exon 1 of 5	3
NDP	ENST00000470584.1	n.456C>T		non_coding_transcript_exon_variant	Exon 3 of 3	2
NDP	ENST00000647044.1	c.*10C>T		3_prime_UTR_variant	Exon 4 of 4			ENSP00000495811.1

Frequencies

GnomAD3 genomes Cov.: 22

GnomAD4 exome AF: 9.50e-7 AC: 1 AN: 1052587 Hom.: 0 Cov.: 28 AF XY: 0.00 AC XY: 0 AN XY: 341631

African (AFR) AF: 0.00 AC: 0 AN: 25028

American (AMR) AF: 0.00 AC: 0 AN: 28197

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 18628

East Asian (EAS) AF: 0.00 AC: 0 AN: 27358

South Asian (SAS) AF: 0.00 AC: 0 AN: 49901

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 37828

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 4082

European-Non Finnish (NFE) AF: 0.00000122 AC: 1 AN: 817181

Other (OTH) AF: 0.00 AC: 0 AN: 44384

GnomAD4 genome Cov.: 22

Alfa AF: 0.00 Hom.: 2

Bravo AF: 0.00000378

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.79
CADD	Benign	1.3
DANN	Benign	0.88
PhyloP100		-0.061

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: rs140653237; hg19: chrX-43809035;