rs366476

Positions:

• chr14-88468307-G-A
• chr14-88468307-G-C

Variant summary

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

The ENST00000556564.6(PTPN21):​c.3397-42C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.432 in 1,538,546 control chromosomes in the GnomAD database, including 146,574 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 0.44 (15047 hom., cov: 32)
  • Exomes 𝑓: 0.43 (131527 hom.)
• Consequence: PTPN21 ENST00000556564.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.36

Genes affected

PTPN21 (HGNC:9651): (protein tyrosine phosphatase non-receptor type 21) 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 contains an N-terminal domain, similar to cytoskeletal- associated proteins including band 4.1, ezrin, merlin, and radixin. This PTP was shown to specially interact with BMX/ETK, a member of Tec tyrosine kinase family characterized by a multimodular structures including PH, SH3, and SH2 domains. The interaction of this PTP with BMX kinase was found to increase the activation of STAT3, but not STAT2 kinase. Studies of the similar gene in mice suggested the possible roles of this PTP in liver regeneration and spermatogenesis. [provided by RefSeq, Jul 2008]

SPATA7 (HGNC:20423): (spermatogenesis associated 7) This gene, originally isolated from testis, is also expressed in retina. Mutations in this gene are associated with Leber congenital amaurosis and juvenile retinitis pigmentosa. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.88).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.567 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
PTPN21	NM_007039.4	c.3397-42C>T		intron_variant		ENST00000556564.6	NP_008970.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
PTPN21	ENST00000556564.6	c.3397-42C>T		intron_variant		1	NM_007039.4	ENSP00000452414	P1

Frequencies

GnomAD3 genomes AF: 0.441 AC: 66971 AN: 151848 Hom.: 15022 Cov.: 32

Gnomad AFR AF: 0.434

Gnomad AMI AF: 0.477

Gnomad AMR AF: 0.528

Gnomad ASJ AF: 0.349

Gnomad EAS AF: 0.584

Gnomad SAS AF: 0.459

Gnomad FIN AF: 0.478

Gnomad MID AF: 0.275

Gnomad NFE AF: 0.414

Gnomad OTH AF: 0.405

GnomAD3 exomes AF: 0.471 AC: 101216 AN: 215122 Hom.: 24365 AF XY: 0.465 AC XY: 54248 AN XY: 116762

Gnomad AFR exome AF: 0.440

Gnomad AMR exome AF: 0.630

Gnomad ASJ exome AF: 0.362

Gnomad EAS exome AF: 0.590

Gnomad SAS exome AF: 0.483

Gnomad FIN exome AF: 0.488

Gnomad NFE exome AF: 0.420

Gnomad OTH exome AF: 0.449

GnomAD4 exome AF: 0.431 AC: 598031 AN: 1386580 Hom.: 131527 Cov.: 31 AF XY: 0.432 AC XY: 297234 AN XY: 688206

Gnomad4 AFR exome AF: 0.428

Gnomad4 AMR exome AF: 0.610

Gnomad4 ASJ exome AF: 0.349

Gnomad4 EAS exome AF: 0.649

Gnomad4 SAS exome AF: 0.476

Gnomad4 FIN exome AF: 0.481

Gnomad4 NFE exome AF: 0.414

Gnomad4 OTH exome AF: 0.431

GnomAD4 genome AF: 0.441 AC: 67049 AN: 151966 Hom.: 15047 Cov.: 32 AF XY: 0.448 AC XY: 33273 AN XY: 74270

Gnomad4 AFR AF: 0.434

Gnomad4 AMR AF: 0.528

Gnomad4 ASJ AF: 0.349

Gnomad4 EAS AF: 0.585

Gnomad4 SAS AF: 0.458

Gnomad4 FIN AF: 0.478

Gnomad4 NFE AF: 0.414

Gnomad4 OTH AF: 0.412

Alfa AF: 0.419 Hom.: 19504

Bravo AF: 0.447

Asia WGS AF: 0.545 AC: 1897 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.88
CADD	Benign	0.043
DANN	Benign	0.73

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: rs366476; hg19: chr14-88934651;