rs1464510

Variant names:

• chr3-188394766-C-A
• rs1464510
• NM_001375462.1:c.-9-11346C>A

Your query was ambiguous. Multiple possible variants found:

• chr3-188394766-C-A
• chr3-188394766-C-G
• chr3-188394766-C-T

Variant summary

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

The NM_001375462.1(LPP):​c.-9-11346C>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.408 in 151,940 control chromosomes in the GnomAD database, including 13,650 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 0.41 (13650 hom., cov: 32)
• Consequence: LPP NM_001375462.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0370
• Publications: 68 publications found

Genes affected

LPP (HGNC:6679): (LIM domain containing preferred translocation partner in lipoma) This gene encodes a member of a subfamily of LIM domain proteins that are characterized by an N-terminal proline-rich region and three C-terminal LIM domains. The encoded protein localizes to the cell periphery in focal adhesions and may be involved in cell-cell adhesion and cell motility. This protein also shuttles through the nucleus and may function as a transcriptional co-activator. This gene is located at the junction of certain disease-related chromosomal translocations, which result in the expression of chimeric proteins that may promote tumor growth. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.65).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.595 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
LPP	NM_001375462.1	c.-9-11346C>A		intron_variant	Intron 3 of 11	ENST00000617246.5	NP_001362391.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
LPP	ENST00000617246.5	c.-9-11346C>A		intron_variant	Intron 3 of 11	1	NM_001375462.1	ENSP00000478901.1

Frequencies

GnomAD3 genomes AF: 0.408 AC: 61897 AN: 151822 Hom.: 13642 Cov.: 32

Gnomad AFR AF: 0.236

Gnomad AMI AF: 0.338

Gnomad AMR AF: 0.473

Gnomad ASJ AF: 0.430

Gnomad EAS AF: 0.613

Gnomad SAS AF: 0.509

Gnomad FIN AF: 0.568

Gnomad MID AF: 0.291

Gnomad NFE AF: 0.450

Gnomad OTH AF: 0.434

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

GnomAD4 genome AF: 0.408 AC: 61935 AN: 151940 Hom.: 13650 Cov.: 32 AF XY: 0.415 AC XY: 30828 AN XY: 74228

African (AFR) AF: 0.236 AC: 9771 AN: 41450

American (AMR) AF: 0.474 AC: 7240 AN: 15288

Ashkenazi Jewish (ASJ) AF: 0.430 AC: 1492 AN: 3466

East Asian (EAS) AF: 0.613 AC: 3161 AN: 5158

South Asian (SAS) AF: 0.510 AC: 2458 AN: 4820

European-Finnish (FIN) AF: 0.568 AC: 5962 AN: 10500

Middle Eastern (MID) AF: 0.299 AC: 88 AN: 294

European-Non Finnish (NFE) AF: 0.450 AC: 30543 AN: 67940

Other (OTH) AF: 0.431 AC: 912 AN: 2114

Alfa AF: 0.438 Hom.: 53766

Bravo AF: 0.396

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.65
CADD	Benign	9.0
DANN	Benign	0.68
PhyloP100		-0.037
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: rs1464510; hg19: chr3-188112554;