15-22853498-C-T

Variant summary

Our verdict is Benign. Variant got -14 ACMG points: 0P and 14B. BP4_Strong BP6_Moderate BA1

The NM_030922.7(NIPA2):c.196+230C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0726 in 151,242 control chromosomes in the GnomAD database, including 741 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★).

• Frequency: Genomes: 𝑓 0.073 (741 hom., cov: 28)
• Consequence: NIPA2 NM_030922.7 intron
• Clinical Significance: Benign criteria provided, single submitter B:1
• Conservation: PhyloP100: -2.10

Genes affected

NIPA2 (HGNC:17044): (NIPA magnesium transporter 2) This gene encodes a possible magnesium transporter. This gene is located adjacent to the imprinted domain in the Prader-Willi syndrome deletion region of chromosome 15. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 3, 7 and 21.[provided by RefSeq, May 2010]

ACMG classification

Verdict is Benign. Variant got -14 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.02).
• BP6: Variant 15-22853498-C-T is Benign according to our data. Variant chr15-22853498-C-T is described in ClinVar as [Benign]. Clinvar id is 1220955.Status of the report is criteria_provided_single_submitter, 1 stars.
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.176 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
NIPA2	NM_030922.7	c.196+230C>T		intron_variant		ENST00000337451.8

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
NIPA2	ENST00000337451.8	c.196+230C>T		intron_variant		5	NM_030922.7	P1

Frequencies

GnomAD3 genomes AF: 0.0725 AC: 10951 AN: 151124 Hom.: 738 Cov.: 28

Gnomad AFR AF: 0.180

Gnomad AMI AF: 0.0330

Gnomad AMR AF: 0.0435

Gnomad ASJ AF: 0.0859

Gnomad EAS AF: 0.000390

Gnomad SAS AF: 0.0224

Gnomad FIN AF: 0.0423

Gnomad MID AF: 0.127

Gnomad NFE AF: 0.0273

Gnomad OTH AF: 0.0713

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.0726 AC: 10973 AN: 151242 Hom.: 741 Cov.: 28 AF XY: 0.0725 AC XY: 5353 AN XY: 73880

Gnomad4 AFR AF: 0.180

Gnomad4 AMR AF: 0.0434

Gnomad4 ASJ AF: 0.0859

Gnomad4 EAS AF: 0.000391

Gnomad4 SAS AF: 0.0226

Gnomad4 FIN AF: 0.0423

Gnomad4 NFE AF: 0.0273

Gnomad4 OTH AF: 0.0705

Alfa AF: 0.0630 Hom.: 76

Bravo AF: 0.0778

Asia WGS AF: 0.0200 AC: 71 AN: 3478

ClinVar

Significance: Benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

Submissions by phenotype

not provided Benign:1

Benign, criteria provided, single submitter

clinical testing

GeneDx

Jun 20, 2021

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Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
Cadd	Benign	0.36
Dann	Benign	0.49

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

LitVar

Other links and lift over

dbSNP: rs28489231; hg19: chr15-23019570;