rs10490775

chr3-62051050-C-T

Variant summary

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

The NM_002841.4(PTPRG):c.520-27113C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.126 in 152,130 control chromosomes in the GnomAD database, including 1,303 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 0.13 (1303 hom., cov: 32)
• Consequence: PTPRG NM_002841.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.85

Genes affected

PTPRG (HGNC:9671): (protein tyrosine phosphatase receptor type G) 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 two tandem intracytoplasmic catalytic domains, and thus represents a receptor-type PTP. The extracellular region of this PTP contains a carbonic anhydrase-like (CAH) domain, which is also found in the extracellular region of PTPRBETA/ZETA. This gene is located in a chromosomal region that is frequently deleted in renal cell carcinoma and lung carcinoma, thus is thought to be a candidate tumor suppressor gene. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.202 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
PTPRG	NM_002841.4	c.520-27113C>T		intron_variant		ENST00000474889.6

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
PTPRG	ENST00000474889.6	c.520-27113C>T		intron_variant		1	NM_002841.4	A1
PTPRG	ENST00000295874.14	c.520-27113C>T		intron_variant		1		P4

Frequencies

GnomAD3 genomes AF: 0.126 AC: 19182 AN: 152012 Hom.: 1305 Cov.: 32

Gnomad AFR AF: 0.145

Gnomad AMI AF: 0.194

Gnomad AMR AF: 0.0980

Gnomad ASJ AF: 0.0792

Gnomad EAS AF: 0.0870

Gnomad SAS AF: 0.212

Gnomad FIN AF: 0.0743

Gnomad MID AF: 0.0892

Gnomad NFE AF: 0.128

Gnomad OTH AF: 0.122

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

GnomAD4 genome AF: 0.126 AC: 19194 AN: 152130 Hom.: 1303 Cov.: 32 AF XY: 0.124 AC XY: 9223 AN XY: 74352

Gnomad4 AFR AF: 0.145

Gnomad4 AMR AF: 0.0982

Gnomad4 ASJ AF: 0.0792

Gnomad4 EAS AF: 0.0868

Gnomad4 SAS AF: 0.212

Gnomad4 FIN AF: 0.0743

Gnomad4 NFE AF: 0.128

Gnomad4 OTH AF: 0.119

Alfa AF: 0.127 Hom.: 1964

Bravo AF: 0.127

Asia WGS AF: 0.133 AC: 465 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
Cadd	Benign	0.13
Dann	Benign	0.67

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: rs10490775; hg19: chr3-62036724;