rs11187074

chr10-92567189-C-Gchr10-92567189-C-T

Variant summary

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

The NM_004969.4(IDE):c.98+6733G>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.849 in 152,154 control chromosomes in the GnomAD database, including 55,063 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 0.85 (55063 hom., cov: 31)
• Consequence: IDE NM_004969.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.329

Genes affected

IDE (HGNC:5381): (insulin degrading enzyme) This gene encodes a zinc metallopeptidase that degrades intracellular insulin, and thereby terminates insulins activity, as well as participating in intercellular peptide signalling by degrading diverse peptides such as glucagon, amylin, bradykinin, and kallidin. The preferential affinity of this enzyme for insulin results in insulin-mediated inhibition of the degradation of other peptides such as beta-amyloid. Deficiencies in this protein's function are associated with Alzheimer's disease and type 2 diabetes mellitus but mutations in this gene have not been shown to be causitive for these diseases. This protein localizes primarily to the cytoplasm but in some cell types localizes to the extracellular space, cell membrane, peroxisome, and mitochondrion. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional transcript variants have been described but have not been experimentally verified.[provided by RefSeq, Sep 2009]

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 = 0.924 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
IDE	NM_004969.4	c.98+6733G>C		intron_variant		ENST00000265986.11

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
IDE	ENST00000265986.11	c.98+6733G>C		intron_variant		1	NM_004969.4	P1

Frequencies

GnomAD3 genomes AF: 0.849 AC: 129019 AN: 152036 Hom.: 55015 Cov.: 31

Gnomad AFR AF: 0.932

Gnomad AMI AF: 0.857

Gnomad AMR AF: 0.807

Gnomad ASJ AF: 0.863

Gnomad EAS AF: 0.919

Gnomad SAS AF: 0.841

Gnomad FIN AF: 0.860

Gnomad MID AF: 0.759

Gnomad NFE AF: 0.801

Gnomad OTH AF: 0.823

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

GnomAD4 genome AF: 0.849 AC: 129124 AN: 152154 Hom.: 55063 Cov.: 31 AF XY: 0.849 AC XY: 63183 AN XY: 74392

Gnomad4 AFR AF: 0.932

Gnomad4 AMR AF: 0.807

Gnomad4 ASJ AF: 0.863

Gnomad4 EAS AF: 0.919

Gnomad4 SAS AF: 0.841

Gnomad4 FIN AF: 0.860

Gnomad4 NFE AF: 0.801

Gnomad4 OTH AF: 0.822

Alfa AF: 0.828 Hom.: 6489

Bravo AF: 0.849

Asia WGS AF: 0.874 AC: 3038 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	1.3
Dann	Benign	0.51

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: rs11187074; hg19: chr10-94326946;