chr8-111564236-T-C

Variant names:

• chr8-111564236-T-C
• rs2352162
• ENST00000524236.2:n.481+21252T>C

Variant summary

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

The ENST00000524236.2(LINC02237):​n.481+21252T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.357 in 151,782 control chromosomes in the GnomAD database, including 11,288 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 0.36 (11288 hom., cov: 30)
• Consequence: LINC02237 ENST00000524236.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.231
• Publications: 0 publications found

Genes affected

LINC02237 (HGNC:53108): (long intergenic non-protein coding RNA 2237)

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.84).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.483 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000524236.2. 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

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	LINC02237	ENST00000524236.2	TSL:3	n.481+21252T>C		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.357 AC: 54190 AN: 151664 Hom.: 11291 Cov.: 30

Gnomad AFR AF: 0.154

Gnomad AMI AF: 0.553

Gnomad AMR AF: 0.311

Gnomad ASJ AF: 0.416

Gnomad EAS AF: 0.156

Gnomad SAS AF: 0.312

Gnomad FIN AF: 0.451

Gnomad MID AF: 0.579

Gnomad NFE AF: 0.488

Gnomad OTH AF: 0.391

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

GnomAD4 genome AF: 0.357 AC: 54187 AN: 151782 Hom.: 11288 Cov.: 30 AF XY: 0.352 AC XY: 26132 AN XY: 74134

African (AFR) AF: 0.154 AC: 6381 AN: 41424

American (AMR) AF: 0.310 AC: 4727 AN: 15244

Ashkenazi Jewish (ASJ) AF: 0.416 AC: 1441 AN: 3468

East Asian (EAS) AF: 0.156 AC: 803 AN: 5146

South Asian (SAS) AF: 0.312 AC: 1499 AN: 4798

European-Finnish (FIN) AF: 0.451 AC: 4723 AN: 10480

Middle Eastern (MID) AF: 0.585 AC: 172 AN: 294

European-Non Finnish (NFE) AF: 0.488 AC: 33125 AN: 67922

Other (OTH) AF: 0.388 AC: 814 AN: 2098

Alfa AF: 0.393 Hom.: 1696

Bravo AF: 0.340

Asia WGS AF: 0.245 AC: 850 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.84
CADD	Benign	1.8
DANN	Benign	0.62
PhyloP100		0.23

Splicing

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

Other links and lift over

dbSNP: rs2352162; hg19: chr8-112576465;