rs10993429

Variant names:

• chr9-94977183-C-T
• rs10993429
• NM_001193329.3:c.1917-2184C>T

Variant summary

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

The NM_001193329.3(AOPEP):​c.1917-2184C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0776 in 152,116 control chromosomes in the GnomAD database, including 1,149 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 0.078 (1149 hom., cov: 32)
• Consequence: AOPEP NM_001193329.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.846

Genes affected

AOPEP (HGNC:1361): (aminopeptidase O (putative)) This gene encodes a member of the M1 zinc aminopeptidase family. The encoded protein is a zinc-dependent metallopeptidase that catalyzes the removal of an amino acid from the amino terminus of a protein or peptide. This protein may play a role in the generation of angiotensin IV. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Oct 2010]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.222 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
AOPEP	NM_001193329.3	c.1917-2184C>T		intron_variant	Intron 10 of 16	ENST00000375315.8	NP_001180258.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
AOPEP	ENST00000375315.8	c.1917-2184C>T		intron_variant	Intron 10 of 16	1	NM_001193329.3	ENSP00000364464.2

Frequencies

GnomAD3 genomes AF: 0.0774 AC: 11760 AN: 151998 Hom.: 1142 Cov.: 32

Gnomad AFR AF: 0.226

Gnomad AMI AF: 0.00658

Gnomad AMR AF: 0.0341

Gnomad ASJ AF: 0.0331

Gnomad EAS AF: 0.105

Gnomad SAS AF: 0.0570

Gnomad FIN AF: 0.00386

Gnomad MID AF: 0.0601

Gnomad NFE AF: 0.0117

Gnomad OTH AF: 0.0516

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

GnomAD4 genome AF: 0.0776 AC: 11802 AN: 152116 Hom.: 1149 Cov.: 32 AF XY: 0.0757 AC XY: 5632 AN XY: 74380

Gnomad4 AFR AF: 0.226

Gnomad4 AMR AF: 0.0341

Gnomad4 ASJ AF: 0.0331

Gnomad4 EAS AF: 0.106

Gnomad4 SAS AF: 0.0573

Gnomad4 FIN AF: 0.00386

Gnomad4 NFE AF: 0.0117

Gnomad4 OTH AF: 0.0511

Alfa AF: 0.0267 Hom.: 235

Bravo AF: 0.0867

Asia WGS AF: 0.108 AC: 376 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	0.54
DANN	Benign	0.43

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: rs10993429; hg19: chr9-97739465;