rs7502935

chr17-78882547-G-A

Variant summary

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

The NM_003255.5(TIMP2):c.131-8628C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.257 in 152,214 control chromosomes in the GnomAD database, including 6,054 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 0.26 (6054 hom., cov: 34)
• Consequence: TIMP2 NM_003255.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.14

Genes affected

TIMP2 (HGNC:11821): (TIMP metallopeptidase inhibitor 2) This gene is a member of the TIMP gene family. The proteins encoded by this gene family are natural inhibitors of the matrix metalloproteinases, a group of peptidases involved in degradation of the extracellular matrix. In addition to an inhibitory role against metalloproteinases, the encoded protein has a unique role among TIMP family members in its ability to directly suppress the proliferation of endothelial cells. As a result, the encoded protein may be critical to the maintenance of tissue homeostasis by suppressing the proliferation of quiescent tissues in response to angiogenic factors, and by inhibiting protease activity in tissues undergoing remodelling of the extracellular matrix. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.82).
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.386 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
TIMP2	NM_003255.5	c.131-8628C>T		intron_variant		ENST00000262768.11

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
TIMP2	ENST00000262768.11	c.131-8628C>T		intron_variant		1	NM_003255.5	P1
TIMP2	ENST00000536189.6	c.-101-8628C>T		intron_variant		2
TIMP2	ENST00000586713.6	c.-101-8628C>T		intron_variant		3

Frequencies

GnomAD3 genomes AF: 0.257 AC: 39063 AN: 152094 Hom.: 6037 Cov.: 34

Gnomad AFR AF: 0.0807

Gnomad AMI AF: 0.360

Gnomad AMR AF: 0.393

Gnomad ASJ AF: 0.329

Gnomad EAS AF: 0.352

Gnomad SAS AF: 0.245

Gnomad FIN AF: 0.326

Gnomad MID AF: 0.218

Gnomad NFE AF: 0.311

Gnomad OTH AF: 0.262

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

GnomAD4 genome AF: 0.257 AC: 39086 AN: 152214 Hom.: 6054 Cov.: 34 AF XY: 0.260 AC XY: 19325 AN XY: 74424

Gnomad4 AFR AF: 0.0805

Gnomad4 AMR AF: 0.394

Gnomad4 ASJ AF: 0.329

Gnomad4 EAS AF: 0.352

Gnomad4 SAS AF: 0.245

Gnomad4 FIN AF: 0.326

Gnomad4 NFE AF: 0.312

Gnomad4 OTH AF: 0.259

Alfa AF: 0.297 Hom.: 3874

Bravo AF: 0.256

Asia WGS AF: 0.311 AC: 1076 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.82
Cadd	Benign	5.0
Dann	Benign	0.65

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: rs7502935; hg19: chr17-76878629;