ENST00000647615.1:n.87-69C>G

Variant names:

• chr16-86715176-C-G
• rs177267
• ENST00000647615.1:n.87-69C>G

Variant summary

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

The ENST00000647615.1(LINC02188):​n.87-69C>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.291 in 151,876 control chromosomes in the GnomAD database, including 6,734 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 (6734 hom., cov: 31)
• Consequence: LINC02188 ENST00000647615.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.298
• Publications: 3 publications found

Genes affected

LINC02188 (HGNC:53050): (long intergenic non-protein coding RNA 2188)

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 (EAS) allele frequency at 95% confidence interval = 0.355 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000647615.1. 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
	LINC02188	ENST00000647615.1		n.87-69C>G		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.291 AC: 44208 AN: 151758 Hom.: 6732 Cov.: 31

Gnomad AFR AF: 0.195

Gnomad AMI AF: 0.247

Gnomad AMR AF: 0.326

Gnomad ASJ AF: 0.238

Gnomad EAS AF: 0.369

Gnomad SAS AF: 0.275

Gnomad FIN AF: 0.366

Gnomad MID AF: 0.245

Gnomad NFE AF: 0.329

Gnomad OTH AF: 0.285

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

GnomAD4 genome AF: 0.291 AC: 44232 AN: 151876 Hom.: 6734 Cov.: 31 AF XY: 0.293 AC XY: 21776 AN XY: 74206

African (AFR) AF: 0.196 AC: 8102 AN: 41436

American (AMR) AF: 0.326 AC: 4973 AN: 15270

Ashkenazi Jewish (ASJ) AF: 0.238 AC: 827 AN: 3470

East Asian (EAS) AF: 0.369 AC: 1899 AN: 5146

South Asian (SAS) AF: 0.274 AC: 1317 AN: 4802

European-Finnish (FIN) AF: 0.366 AC: 3844 AN: 10514

Middle Eastern (MID) AF: 0.240 AC: 70 AN: 292

European-Non Finnish (NFE) AF: 0.329 AC: 22377 AN: 67928

Other (OTH) AF: 0.284 AC: 598 AN: 2108

Alfa AF: 0.311 Hom.: 927

Bravo AF: 0.285

Asia WGS AF: 0.329 AC: 1143 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	6.3
DANN	Benign	0.87
PhyloP100		0.30

Splicing

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

Other links and lift over

dbSNP: rs177267; hg19: chr16-86748782;