20-23637934-T-G

Position:

• chr20-23637934-T-G

Variant summary

Our verdict is Benign. Variant got -20 ACMG points: 0P and 20B. BP4_Strong BP6_Very_Strong BA1

The NM_000099.4(CST3):​c.-72A>C variant causes a 5 prime UTR change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.224 in 1,270,140 control chromosomes in the GnomAD database, including 31,148 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★★).

• Frequency:
  • Genomes: 𝑓 0.20 (3304 hom., cov: 31)
  • Exomes 𝑓: 0.23 (27844 hom.)
• Consequence: CST3 NM_000099.4 5_prime_UTR
• Scores: Splicing: ADA: 0.00001103
• Clinical Significance: Benign criteria provided, multiple submitters, no conflicts B:2
• Conservation: PhyloP100: -3.54

Genes affected

CST3 (HGNC:2475): (cystatin C) The cystatin superfamily encompasses proteins that contain multiple cystatin-like sequences. Some of the members are active cysteine protease inhibitors, while others have lost or perhaps never acquired this inhibitory activity. There are three inhibitory families in the superfamily, including the type 1 cystatins (stefins), type 2 cystatins and the kininogens. The type 2 cystatin proteins are a class of cysteine proteinase inhibitors found in a variety of human fluids and secretions, where they appear to provide protective functions. The cystatin locus on chromosome 20 contains the majority of the type 2 cystatin genes and pseudogenes. This gene is located in the cystatin locus and encodes the most abundant extracellular inhibitor of cysteine proteases, which is found in high concentrations in biological fluids and is expressed in virtually all organs of the body. A mutation in this gene has been associated with amyloid angiopathy. Expression of this protein in vascular wall smooth muscle cells is severely reduced in both atherosclerotic and aneurysmal aortic lesions, establishing its role in vascular disease. In addition, this protein has been shown to have an antimicrobial function, inhibiting the replication of herpes simplex virus. Alternative splicing results in multiple transcript variants encoding a single protein. [provided by RefSeq, Nov 2014]

ACMG classification

Verdict is Benign. Variant got -20 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.79).
• BP6: Variant 20-23637934-T-G is Benign according to our data. Variant chr20-23637934-T-G is described in ClinVar as [Benign]. Clinvar id is 402569.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.31 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
CST3	NM_000099.4	c.-72A>C		5_prime_UTR_variant	1/3	ENST00000376925.8	NP_000090.1
CST3	NM_001288614.2	c.-72A>C		5_prime_UTR_variant	1/4		NP_001275543.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
CST3	ENST00000376925.8	c.-72A>C		5_prime_UTR_variant	1/3	1	NM_000099.4	ENSP00000366124.3
CST3	ENST00000398411.5	c.-72A>C		5_prime_UTR_variant	1/4	1		ENSP00000381448.1
CST3	ENST00000398409.1	c.-70-2A>C		splice_acceptor_variant, intron_variant		3		ENSP00000381446.1

Frequencies

GnomAD3 genomes AF: 0.205 AC: 30722 AN: 150196 Hom.: 3306 Cov.: 31

Gnomad AFR AF: 0.215

Gnomad AMI AF: 0.0910

Gnomad AMR AF: 0.133

Gnomad ASJ AF: 0.163

Gnomad EAS AF: 0.140

Gnomad SAS AF: 0.325

Gnomad FIN AF: 0.231

Gnomad MID AF: 0.150

Gnomad NFE AF: 0.210

Gnomad OTH AF: 0.192

GnomAD4 exome AF: 0.227 AC: 253908 AN: 1119832 Hom.: 27844 Cov.: 31 AF XY: 0.229 AC XY: 123478 AN XY: 539788

Gnomad4 AFR exome AF: 0.241

Gnomad4 AMR exome AF: 0.152

Gnomad4 ASJ exome AF: 0.202

Gnomad4 EAS exome AF: 0.175

Gnomad4 SAS exome AF: 0.312

Gnomad4 FIN exome AF: 0.283

Gnomad4 NFE exome AF: 0.223

Gnomad4 OTH exome AF: 0.227

GnomAD4 genome AF: 0.204 AC: 30723 AN: 150308 Hom.: 3304 Cov.: 31 AF XY: 0.205 AC XY: 15070 AN XY: 73402

Gnomad4 AFR AF: 0.215

Gnomad4 AMR AF: 0.133

Gnomad4 ASJ AF: 0.163

Gnomad4 EAS AF: 0.140

Gnomad4 SAS AF: 0.324

Gnomad4 FIN AF: 0.231

Gnomad4 NFE AF: 0.210

Gnomad4 OTH AF: 0.189

Alfa AF: 0.146 Hom.: 479

Bravo AF: 0.190

Asia WGS AF: 0.183 AC: 633 AN: 3462

ClinVar

Significance: Benign

Submissions summary: Benign:2

Revision: criteria provided, multiple submitters, no conflicts

Submissions by phenotype

not specified Benign:1

Benign, criteria provided, single submitter

clinical testing

Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

Mar 28, 2016

Variant identified in a genome or exome case(s) and assessed due to predicted null impact of the variant or pathogenic assertions in the literature or databases. Disclaimer: This variant has not undergone full assessment. The following are preliminary notes: Frequency in 1000Genomes: 410/2178=18.8% -

not provided Benign:1

Benign, criteria provided, single submitter

not provided

Breakthrough Genomics, Breakthrough Genomics

-

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.79
CADD	Benign	2.0
DANN	Benign	0.41

Splicing

Name	Calibrated prediction	Score	Prediction
dbscSNV1_ADA	Benign	0.000011
dbscSNV1_RF	Benign	0.0
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: rs73318135; hg19: chr20-23618571;