chr11-104517986-T-G

Variant names:

• chr11-104517986-T-G
• rs1487683
• ENST00000536529.5:n.423-5753A>C

Variant summary

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

The ENST00000536529.5(LINC02552):​n.423-5753A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.829 in 151,816 control chromosomes in the GnomAD database, including 52,493 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 0.83 (52493 hom., cov: 29)
• Consequence: LINC02552 ENST00000536529.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0980
• Publications: 2 publications found

Genes affected

LINC02552 (HGNC:53587): (long intergenic non-protein coding RNA 2552)

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.97).
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.889 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000536529.5. 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
There are no transcript annotations for this variant.

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	LINC02552	ENST00000536529.5	TSL:3	n.423-5753A>C		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.829 AC: 125828 AN: 151698 Hom.: 52465 Cov.: 29

Gnomad AFR AF: 0.749

Gnomad AMI AF: 0.859

Gnomad AMR AF: 0.902

Gnomad ASJ AF: 0.820

Gnomad EAS AF: 0.838

Gnomad SAS AF: 0.817

Gnomad FIN AF: 0.819

Gnomad MID AF: 0.842

Gnomad NFE AF: 0.863

Gnomad OTH AF: 0.850

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

GnomAD4 genome AF: 0.829 AC: 125907 AN: 151816 Hom.: 52493 Cov.: 29 AF XY: 0.831 AC XY: 61599 AN XY: 74150

African (AFR) AF: 0.749 AC: 30974 AN: 41364

American (AMR) AF: 0.902 AC: 13759 AN: 15256

Ashkenazi Jewish (ASJ) AF: 0.820 AC: 2848 AN: 3472

East Asian (EAS) AF: 0.837 AC: 4294 AN: 5128

South Asian (SAS) AF: 0.817 AC: 3923 AN: 4800

European-Finnish (FIN) AF: 0.819 AC: 8618 AN: 10522

Middle Eastern (MID) AF: 0.840 AC: 247 AN: 294

European-Non Finnish (NFE) AF: 0.863 AC: 58681 AN: 67966

Other (OTH) AF: 0.847 AC: 1780 AN: 2102

Alfa AF: 0.848 Hom.: 9183

Bravo AF: 0.831

Asia WGS AF: 0.788 AC: 2740 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.97
CADD	Benign	2.0
DANN	Benign	0.60
PhyloP100		-0.098

Splicing

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

Other links and lift over

dbSNP: rs1487683; hg19: chr11-104388714;