rs7313997

Variant names:

• chr12-70872178-A-C
• rs7313997
• NM_002849.4:c.357+20501T>G

Variant summary

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

The NM_002849.4(PTPRR):​c.357+20501T>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.165 in 152,110 control chromosomes in the GnomAD database, including 3,259 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 0.17 (3259 hom., cov: 32)
• Consequence: PTPRR NM_002849.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.84
• Publications: 4 publications found

Genes affected

PTPRR (HGNC:9680): (protein tyrosine phosphatase receptor type R) 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 intracellular catalytic domain, and thus represents a receptor-type PTP. Silencing of this gene has been associated with colorectal cancer. Multiple transcript variants encoding different isoforms have been found for this gene. This gene shares a symbol (PTPRQ) with another gene, protein tyrosine phosphatase, receptor type, Q (GeneID 374462), which is also located on chromosome 12. [provided by RefSeq, May 2011]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.0).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.359 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
PTPRR	NM_002849.4	c.357+20501T>G		intron_variant	Intron 2 of 13	ENST00000283228.7	NP_002840.2
PTPRR	XM_011538615.3	c.333+20501T>G		intron_variant	Intron 2 of 13		XP_011536917.1
PTPRR	XM_047429233.1	c.357+20501T>G		intron_variant	Intron 2 of 11		XP_047285189.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
PTPRR	ENST00000283228.7	c.357+20501T>G		intron_variant	Intron 2 of 13	1	NM_002849.4	ENSP00000283228.2

Frequencies

GnomAD3 genomes AF: 0.165 AC: 25118 AN: 151992 Hom.: 3254 Cov.: 32

Gnomad AFR AF: 0.364

Gnomad AMI AF: 0.105

Gnomad AMR AF: 0.102

Gnomad ASJ AF: 0.0617

Gnomad EAS AF: 0.0410

Gnomad SAS AF: 0.0977

Gnomad FIN AF: 0.0908

Gnomad MID AF: 0.0759

Gnomad NFE AF: 0.0921

Gnomad OTH AF: 0.139

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

GnomAD4 genome AF: 0.165 AC: 25145 AN: 152110 Hom.: 3259 Cov.: 32 AF XY: 0.161 AC XY: 12004 AN XY: 74376

African (AFR) AF: 0.363 AC: 15056 AN: 41422

American (AMR) AF: 0.102 AC: 1559 AN: 15298

Ashkenazi Jewish (ASJ) AF: 0.0617 AC: 214 AN: 3470

East Asian (EAS) AF: 0.0407 AC: 211 AN: 5180

South Asian (SAS) AF: 0.0974 AC: 469 AN: 4816

European-Finnish (FIN) AF: 0.0908 AC: 963 AN: 10602

Middle Eastern (MID) AF: 0.0748 AC: 22 AN: 294

European-Non Finnish (NFE) AF: 0.0921 AC: 6262 AN: 68000

Other (OTH) AF: 0.138 AC: 293 AN: 2116

Alfa AF: 0.115 Hom.: 754

Bravo AF: 0.175

Asia WGS AF: 0.0990 AC: 344 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	0.18
DANN	Benign	0.77
PhyloP100		-1.8
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: rs7313997; hg19: chr12-71265958;