15-73936123-C-T

Variant names:

• chr15-73936123-C-T
• rs893816
• NM_005576.4:c.1103-6731C>T

Variant summary

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

The NM_005576.4(LOXL1):​c.1103-6731C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.286 in 151,846 control chromosomes in the GnomAD database, including 6,843 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 0.29 (6843 hom., cov: 31)
• Consequence: LOXL1 NM_005576.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.849
• Publications: 7 publications found

Genes affected

LOXL1 (HGNC:6665): (lysyl oxidase like 1) This gene encodes a member of the lysyl oxidase family of proteins. The prototypic member of the family is essential to the biogenesis of connective tissue, encoding an extracellular copper-dependent amine oxidase that catalyzes the first step in the formation of crosslinks in collagen and elastin. The encoded preproprotein is proteolytically processed to generate the mature enzyme. A highly conserved amino acid sequence at the C-terminus end appears to be sufficient for amine oxidase activity, suggesting that each family member may retain this function. The N-terminus is poorly conserved and may impart additional roles in developmental regulation, senescence, tumor suppression, cell growth control, and chemotaxis to each member of the family. Mutations in this gene are associated with exfoliation syndrome. [provided by RefSeq, Jan 2016]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.82).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.531 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_005576.4. 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
	LOXL1	NM_005576.4	MANE Select	c.1103-6731C>T		intron	N/A	NP_005567.2	Q08397

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	LOXL1	ENST00000261921.8	TSL:1 MANE Select	c.1103-6731C>T		intron	N/A	ENSP00000261921.7	Q08397
	LOXL1	ENST00000856631.1		c.1103-6731C>T		intron	N/A	ENSP00000526690.1
	LOXL1	ENST00000566011.5	TSL:5	n.1103-5752C>T		intron	N/A	ENSP00000457827.1	H3BUV8

Frequencies

GnomAD3 genomes AF: 0.286 AC: 43401 AN: 151730 Hom.: 6841 Cov.: 31

Gnomad AFR AF: 0.169

Gnomad AMI AF: 0.248

Gnomad AMR AF: 0.323

Gnomad ASJ AF: 0.257

Gnomad EAS AF: 0.548

Gnomad SAS AF: 0.330

Gnomad FIN AF: 0.313

Gnomad MID AF: 0.174

Gnomad NFE AF: 0.324

Gnomad OTH AF: 0.299

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

GnomAD4 genome AF: 0.286 AC: 43417 AN: 151846 Hom.: 6843 Cov.: 31 AF XY: 0.289 AC XY: 21425 AN XY: 74178

African (AFR) AF: 0.168 AC: 6976 AN: 41416

American (AMR) AF: 0.323 AC: 4942 AN: 15280

Ashkenazi Jewish (ASJ) AF: 0.257 AC: 890 AN: 3466

East Asian (EAS) AF: 0.547 AC: 2805 AN: 5124

South Asian (SAS) AF: 0.331 AC: 1589 AN: 4806

European-Finnish (FIN) AF: 0.313 AC: 3301 AN: 10550

Middle Eastern (MID) AF: 0.187 AC: 55 AN: 294

European-Non Finnish (NFE) AF: 0.324 AC: 22002 AN: 67890

Other (OTH) AF: 0.299 AC: 631 AN: 2110

Alfa AF: 0.243 Hom.: 1233

Bravo AF: 0.282

Asia WGS AF: 0.363 AC: 1268 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.82
CADD	Benign	6.8
DANN	Benign	0.44
PhyloP100		0.85
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: rs893816; hg19: chr15-74228464;