1-165533954-A-G

Variant names:

• chr1-165533954-A-G
• rs285424
• ENST00000416424.5:n.873-10867T>C

Variant summary

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

The ENST00000416424.5(LRRC52-AS1):​n.873-10867T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.929 in 152,152 control chromosomes in the GnomAD database, including 66,019 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 0.93 (66019 hom., cov: 30)
• Consequence: LRRC52-AS1 ENST00000416424.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.510
• Publications: 0 publications found

Genes affected

LRRC52-AS1 (HGNC:54044): (LRRC52 antisense RNA 1)

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.87).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.977 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000416424.5. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	LRRC52-AS1	NR_026744.2		n.960-10867T>C		intron	N/A

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	LRRC52-AS1	ENST00000416424.5	TSL:1	n.873-10867T>C		intron	N/A
	LRRC52-AS1	ENST00000438275.5	TSL:1	n.933-5072T>C		intron	N/A
	LRRC52-AS1	ENST00000452283.5	TSL:1	n.178+5481T>C		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.929 AC: 141281 AN: 152034 Hom.: 65971 Cov.: 30

Gnomad AFR AF: 0.828

Gnomad AMI AF: 0.948

Gnomad AMR AF: 0.956

Gnomad ASJ AF: 0.973

Gnomad EAS AF: 1.00

Gnomad SAS AF: 0.951

Gnomad FIN AF: 0.992

Gnomad MID AF: 0.927

Gnomad NFE AF: 0.966

Gnomad OTH AF: 0.937

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

GnomAD4 genome AF: 0.929 AC: 141385 AN: 152152 Hom.: 66019 Cov.: 30 AF XY: 0.931 AC XY: 69285 AN XY: 74390

African (AFR) AF: 0.828 AC: 34312 AN: 41458

American (AMR) AF: 0.957 AC: 14614 AN: 15278

Ashkenazi Jewish (ASJ) AF: 0.973 AC: 3378 AN: 3472

East Asian (EAS) AF: 1.00 AC: 5181 AN: 5182

South Asian (SAS) AF: 0.952 AC: 4575 AN: 4808

European-Finnish (FIN) AF: 0.992 AC: 10515 AN: 10604

Middle Eastern (MID) AF: 0.925 AC: 272 AN: 294

European-Non Finnish (NFE) AF: 0.966 AC: 65699 AN: 68038

Other (OTH) AF: 0.937 AC: 1976 AN: 2108

Alfa AF: 0.928 Hom.: 8887

Bravo AF: 0.922

Asia WGS AF: 0.960 AC: 3339 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.87
CADD	Benign	4.4
DANN	Benign	0.79
PhyloP100		0.51

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs285424; hg19: chr1-165503191;