15-58542176-T-C

Position:

• chr15-58542176-T-C

Variant summary

Our verdict is Benign. Variant got -14 ACMG points: 0P and 14B. BP4_Strong BP6_Moderate BA1

The NM_000236.3(LIPC):​c.456+209T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.287 in 151,848 control chromosomes in the GnomAD database, including 6,599 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★).

• Frequency: Genomes: 𝑓 0.29 (6599 hom., cov: 31)
• Consequence: LIPC NM_000236.3 intron
• Clinical Significance: Benign criteria provided, single submitter B:1
• Conservation: PhyloP100: -0.567

Genes affected

LIPC (HGNC:6619): (lipase C, hepatic type) Enables phospholipase A1 activity and triglyceride lipase activity. Involved in several processes, including lipid homeostasis; plasma lipoprotein particle remodeling; and triglyceride catabolic process. Located in extracellular space. Implicated in several diseases, including Alzheimer's disease; coronary artery disease; familial combined hyperlipidemia; peripheral vascular disease; and type 2 diabetes mellitus. Biomarker of hyperinsulinism; obesity; and type 1 diabetes mellitus. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Verdict is Benign. Variant got -14 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.86).
• BP6: Variant 15-58542176-T-C is Benign according to our data. Variant chr15-58542176-T-C is described in ClinVar as [Benign]. Clinvar id is 1225442.Status of the report is criteria_provided_single_submitter, 1 stars.
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.442 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
LIPC	NM_000236.3	c.456+209T>C		intron_variant		ENST00000299022.10

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
LIPC	ENST00000299022.10	c.456+209T>C		intron_variant		1	NM_000236.3	P1

Frequencies

GnomAD3 genomes AF: 0.287 AC: 43477 AN: 151730 Hom.: 6590 Cov.: 31

Gnomad AFR AF: 0.255

Gnomad AMI AF: 0.237

Gnomad AMR AF: 0.379

Gnomad ASJ AF: 0.252

Gnomad EAS AF: 0.457

Gnomad SAS AF: 0.382

Gnomad FIN AF: 0.367

Gnomad MID AF: 0.313

Gnomad NFE AF: 0.255

Gnomad OTH AF: 0.281

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

GnomAD4 genome AF: 0.287 AC: 43523 AN: 151848 Hom.: 6599 Cov.: 31 AF XY: 0.295 AC XY: 21848 AN XY: 74180

Gnomad4 AFR AF: 0.255

Gnomad4 AMR AF: 0.380

Gnomad4 ASJ AF: 0.252

Gnomad4 EAS AF: 0.457

Gnomad4 SAS AF: 0.383

Gnomad4 FIN AF: 0.367

Gnomad4 NFE AF: 0.255

Gnomad4 OTH AF: 0.281

Alfa AF: 0.108 Hom.: 175

Bravo AF: 0.286

Asia WGS AF: 0.423 AC: 1469 AN: 3478

ClinVar

Significance: Benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

Submissions by phenotype

not provided Benign:1

Benign, criteria provided, single submitter

clinical testing

GeneDx

Aug 30, 2018

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.86
CADD	Benign	1.6
DANN	Benign	0.84

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: rs2242061; hg19: chr15-58834375;