10-92544375-C-T

Variant names:

• chr10-92544375-C-T
• rs11187060
• NM_004969.4:c.99-6825G>A

Variant summary

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

The NM_004969.4(IDE):​c.99-6825G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.332 in 151,912 control chromosomes in the GnomAD database, including 8,553 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 0.33 (8553 hom., cov: 32)
• Consequence: IDE NM_004969.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.187
• Publications: 18 publications found

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

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.88).
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.374 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_004969.4. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	IDE	NM_004969.4	MANE Select	c.99-6825G>A		intron	N/A	NP_004960.2	P14735-1
	IDE	NM_001322793.2		c.99-6825G>A		intron	N/A	NP_001309722.1	A0A3B3ISG5
	IDE	NM_001322794.2		c.99-6825G>A		intron	N/A	NP_001309723.1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	IDE	ENST00000265986.11	TSL:1 MANE Select	c.99-6825G>A		intron	N/A	ENSP00000265986.6	P14735-1
	IDE	ENST00000478361.6	TSL:1	n.*309-6825G>A		intron	N/A	ENSP00000473506.1	R4GN65
	IDE	ENST00000971392.1		c.99-6825G>A		intron	N/A	ENSP00000641451.1

Frequencies

GnomAD3 genomes AF: 0.332 AC: 50352 AN: 151794 Hom.: 8538 Cov.: 32

Gnomad AFR AF: 0.304

Gnomad AMI AF: 0.195

Gnomad AMR AF: 0.383

Gnomad ASJ AF: 0.279

Gnomad EAS AF: 0.204

Gnomad SAS AF: 0.305

Gnomad FIN AF: 0.424

Gnomad MID AF: 0.272

Gnomad NFE AF: 0.340

Gnomad OTH AF: 0.310

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

GnomAD4 genome AF: 0.332 AC: 50398 AN: 151912 Hom.: 8553 Cov.: 32 AF XY: 0.336 AC XY: 24910 AN XY: 74228

African (AFR) AF: 0.305 AC: 12614 AN: 41418

American (AMR) AF: 0.383 AC: 5841 AN: 15268

Ashkenazi Jewish (ASJ) AF: 0.279 AC: 966 AN: 3464

East Asian (EAS) AF: 0.204 AC: 1056 AN: 5182

South Asian (SAS) AF: 0.305 AC: 1470 AN: 4824

European-Finnish (FIN) AF: 0.424 AC: 4444 AN: 10492

Middle Eastern (MID) AF: 0.282 AC: 83 AN: 294

European-Non Finnish (NFE) AF: 0.340 AC: 23093 AN: 67954

Other (OTH) AF: 0.310 AC: 654 AN: 2108

Alfa AF: 0.329 Hom.: 21469

Bravo AF: 0.326

Asia WGS AF: 0.278 AC: 967 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.88
CADD	Benign	1.4
DANN	Benign	0.64
PhyloP100		-0.19
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: rs11187060; hg19: chr10-94304132;