rs10838801

Variant names:

• chr11-48076728-G-A
• rs10838801
• NM_002843.4:c.97-33330G>A

Your query was ambiguous. Multiple possible variants found:

• chr11-48076728-G-A
• chr11-48076728-G-T

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_002843.4(PTPRJ):​c.97-33330G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.575 in 150,652 control chromosomes in the GnomAD database, including 28,390 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 0.57 (28390 hom., cov: 27)
• Consequence: PTPRJ NM_002843.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.21
• Publications: 26 publications found

Genes affected

PTPRJ (HGNC:9673): (protein tyrosine phosphatase receptor type J) 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 containing five fibronectin type III repeats, a single transmembrane region, and a single intracytoplasmic catalytic domain, and thus represents a receptor-type PTP. This protein is present in all hematopoietic lineages, and was shown to negatively regulate T cell receptor signaling possibly through interfering with the phosphorylation of Phospholipase C Gamma 1 and Linker for Activation of T Cells. This protein can also dephosphorylate the PDGF beta receptor, and may be involved in UV-induced signal transduction. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

PTPRJ Gene-Disease associations (from GenCC):

• hereditary nonpolyposis colon cancer

  Inheritance: AD Classification: LIMITED Submitted by: ClinGen
• thrombocytopenia 10

  Inheritance: AR Classification: LIMITED Submitted by: Ambry Genetics
• colorectal cancer

  Inheritance: Unknown Classification: NO_KNOWN Submitted by: Labcorp Genetics (formerly Invitae)

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.58).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.784 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
PTPRJ	NM_002843.4	c.97-33330G>A		intron_variant	Intron 1 of 24	ENST00000418331.7	NP_002834.3
PTPRJ	NM_001098503.2	c.97-33330G>A		intron_variant	Intron 1 of 8		NP_001091973.1
PTPRJ	XM_017018085.2	c.49-33330G>A		intron_variant	Intron 1 of 24		XP_016873574.1
PTPRJ	XM_047427374.1	c.439-33330G>A		intron_variant	Intron 1 of 16		XP_047283330.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
PTPRJ	ENST00000418331.7	c.97-33330G>A		intron_variant	Intron 1 of 24	1	NM_002843.4	ENSP00000400010.2

Frequencies

GnomAD3 genomes AF: 0.575 AC: 86583 AN: 150546 Hom.: 28381 Cov.: 27

Gnomad AFR AF: 0.236

Gnomad AMI AF: 0.864

Gnomad AMR AF: 0.691

Gnomad ASJ AF: 0.698

Gnomad EAS AF: 0.805

Gnomad SAS AF: 0.772

Gnomad FIN AF: 0.709

Gnomad MID AF: 0.643

Gnomad NFE AF: 0.691

Gnomad OTH AF: 0.627

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

GnomAD4 genome AF: 0.575 AC: 86605 AN: 150652 Hom.: 28390 Cov.: 27 AF XY: 0.581 AC XY: 42688 AN XY: 73476

African (AFR) AF: 0.236 AC: 9683 AN: 41090

American (AMR) AF: 0.692 AC: 10468 AN: 15130

Ashkenazi Jewish (ASJ) AF: 0.698 AC: 2421 AN: 3468

East Asian (EAS) AF: 0.805 AC: 4123 AN: 5124

South Asian (SAS) AF: 0.771 AC: 3663 AN: 4748

European-Finnish (FIN) AF: 0.709 AC: 7158 AN: 10092

Middle Eastern (MID) AF: 0.643 AC: 184 AN: 286

European-Non Finnish (NFE) AF: 0.691 AC: 46806 AN: 67728

Other (OTH) AF: 0.632 AC: 1313 AN: 2076

Alfa AF: 0.642 Hom.: 53840

Bravo AF: 0.562

Asia WGS AF: 0.758 AC: 2633 AN: 3474

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.58
CADD	Benign	12
DANN	Benign	0.68
PhyloP100		1.2
Mutation Taster		=100/0	polymorphism (auto)

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: rs10838801; hg19: chr11-48098280;