NM_001136528.2:c.488-327G>A

Variant names:

• chr2-223992327-C-T
• rs2076924
• NM_001136528.2:c.488-327G>A

Variant summary

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

The NM_001136528.2(SERPINE2):​c.488-327G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.632 in 149,156 control chromosomes in the GnomAD database, including 29,715 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 0.63 (29715 hom., cov: 31)
• Consequence: SERPINE2 NM_001136528.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.213
• Publications: 3 publications found

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

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.95).
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.713 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
SERPINE2	NM_001136528.2	c.488-327G>A		intron_variant	Intron 3 of 8	ENST00000409304.6	NP_001130000.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
SERPINE2	ENST00000409304.6	c.488-327G>A		intron_variant	Intron 3 of 8	1	NM_001136528.2	ENSP00000386412.1

Frequencies

GnomAD3 genomes AF: 0.632 AC: 94247 AN: 149042 Hom.: 29699 Cov.: 31

Gnomad AFR AF: 0.559

Gnomad AMI AF: 0.615

Gnomad AMR AF: 0.724

Gnomad ASJ AF: 0.567

Gnomad EAS AF: 0.454

Gnomad SAS AF: 0.605

Gnomad FIN AF: 0.637

Gnomad MID AF: 0.615

Gnomad NFE AF: 0.673

Gnomad OTH AF: 0.647

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

GnomAD4 genome AF: 0.632 AC: 94297 AN: 149156 Hom.: 29715 Cov.: 31 AF XY: 0.631 AC XY: 45889 AN XY: 72772

African (AFR) AF: 0.559 AC: 22432 AN: 40118

American (AMR) AF: 0.725 AC: 10921 AN: 15068

Ashkenazi Jewish (ASJ) AF: 0.567 AC: 1946 AN: 3430

East Asian (EAS) AF: 0.454 AC: 2252 AN: 4958

South Asian (SAS) AF: 0.606 AC: 2812 AN: 4642

European-Finnish (FIN) AF: 0.637 AC: 6503 AN: 10210

Middle Eastern (MID) AF: 0.606 AC: 177 AN: 292

European-Non Finnish (NFE) AF: 0.673 AC: 45385 AN: 67482

Other (OTH) AF: 0.640 AC: 1320 AN: 2064

Alfa AF: 0.637 Hom.: 3862

Bravo AF: 0.624

Asia WGS AF: 0.482 AC: 1674 AN: 3472

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.95
CADD	Benign	1.2
DANN	Benign	0.57
PhyloP100		0.21
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: rs2076924; hg19: chr2-224857044;