rs7608941

Positions:

• chr2-223989351-C-A
• chr2-223989351-C-G

Variant summary

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

The NM_001136528.2(SERPINE2):​c.685+2452G>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.672 in 152,022 control chromosomes in the GnomAD database, including 35,144 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 0.67 (35144 hom., cov: 32)
• Consequence: SERPINE2 NM_001136528.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.68

Genes affected

SERPINE2 (HGNC:8951): (serpin family E member 2) This gene encodes a member of the serpin family of proteins, a group of proteins that inhibit serine proteases. Thrombin, urokinase, plasmin and trypsin are among the proteases that this family member can inhibit. This gene is a susceptibility gene for chronic obstructive pulmonary disease and for emphysema. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.757 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
SERPINE2	NM_001136528.2	c.685+2452G>T		intron_variant		ENST00000409304.6	NP_001130000.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
SERPINE2	ENST00000409304.6	c.685+2452G>T		intron_variant		1	NM_001136528.2	ENSP00000386412	A1

Frequencies

GnomAD3 genomes AF: 0.672 AC: 102048 AN: 151904 Hom.: 35140 Cov.: 32

Gnomad AFR AF: 0.537

Gnomad AMI AF: 0.842

Gnomad AMR AF: 0.626

Gnomad ASJ AF: 0.590

Gnomad EAS AF: 0.465

Gnomad SAS AF: 0.708

Gnomad FIN AF: 0.782

Gnomad MID AF: 0.554

Gnomad NFE AF: 0.763

Gnomad OTH AF: 0.656

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

GnomAD4 genome AF: 0.672 AC: 102088 AN: 152022 Hom.: 35144 Cov.: 32 AF XY: 0.669 AC XY: 49741 AN XY: 74334

Gnomad4 AFR AF: 0.537

Gnomad4 AMR AF: 0.626

Gnomad4 ASJ AF: 0.590

Gnomad4 EAS AF: 0.466

Gnomad4 SAS AF: 0.708

Gnomad4 FIN AF: 0.782

Gnomad4 NFE AF: 0.763

Gnomad4 OTH AF: 0.652

Alfa AF: 0.717 Hom.: 39444

Bravo AF: 0.652

Asia WGS AF: 0.570 AC: 1984 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	0.082
DANN	Benign	0.48

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: rs7608941; hg19: chr2-224854068;