2-219301232-A-G

Position:

• chr2-219301232-A-G

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_002846.4(PTPRN):​c.1127-255T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0768 in 152,240 control chromosomes in the GnomAD database, including 556 homozygotes. 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: 𝑓 0.077 (556 hom., cov: 33)
• Consequence: PTPRN NM_002846.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.426

Genes affected

PTPRN (HGNC:9676): (protein tyrosine phosphatase receptor type N) The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP possesses an extracellular region, a single transmembrane region, and a single catalytic domain, and thus represents a receptor-type PTP. This PTP was found to be an autoantigen that is reactive with insulin-dependent diabetes mellitus (IDDM) patient sera, and thus may be a potential target of autoimmunity in diabetes mellitus. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Dec 2010]

(HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.86).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.099 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
PTPRN	NM_002846.4	c.1127-255T>C		intron_variant		ENST00000295718.7	NP_002837.1
PTPRN	NM_001199763.2	c.1127-255T>C		intron_variant			NP_001186692.1
PTPRN	NM_001199764.2	c.857-255T>C		intron_variant			NP_001186693.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
PTPRN	ENST00000295718.7	c.1127-255T>C		intron_variant		1	NM_002846.4	ENSP00000295718	P1
	ENST00000417355.1	n.177+808A>G		intron_variant, non_coding_transcript_variant		3

Frequencies

GnomAD3 genomes AF: 0.0768 AC: 11684 AN: 152122 Hom.: 549 Cov.: 33

Gnomad AFR AF: 0.0296

Gnomad AMI AF: 0.175

Gnomad AMR AF: 0.0808

Gnomad ASJ AF: 0.124

Gnomad EAS AF: 0.0456

Gnomad SAS AF: 0.108

Gnomad FIN AF: 0.0762

Gnomad MID AF: 0.120

Gnomad NFE AF: 0.101

Gnomad OTH AF: 0.0856

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

GnomAD4 genome AF: 0.0768 AC: 11689 AN: 152240 Hom.: 556 Cov.: 33 AF XY: 0.0757 AC XY: 5636 AN XY: 74456

Gnomad4 AFR AF: 0.0295

Gnomad4 AMR AF: 0.0807

Gnomad4 ASJ AF: 0.124

Gnomad4 EAS AF: 0.0457

Gnomad4 SAS AF: 0.107

Gnomad4 FIN AF: 0.0762

Gnomad4 NFE AF: 0.101

Gnomad4 OTH AF: 0.0927

Alfa AF: 0.0443 Hom.: 50

Bravo AF: 0.0763

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.86
CADD	Benign	1.1
DANN	Benign	0.47

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

Publications

LitVar

Other links and lift over

dbSNP: rs2292607; hg19: chr2-220165954;