chr6-82095575-G-A

Variant names:

• chr6-82095575-G-A
• rs1342196
• ENST00000660637.1:n.156+6070C>T

Variant summary

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

The NR_149135.1(LINC02542):​n.206+5985C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.281 in 152,018 control chromosomes in the GnomAD database, including 6,211 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 0.28 (6211 hom., cov: 32)
• Consequence: LINC02542 NR_149135.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0990
• Publications: 3 publications found

Genes affected

LINC02542 (HGNC:53576): (long intergenic non-protein coding RNA 2542)

ENSG00000306836 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.356 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NR_149135.1. 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
	LINC02542	NR_149135.1		n.206+5985C>T		intron	N/A

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	LINC02542	ENST00000660637.1		n.156+6070C>T		intron	N/A
	LINC02542	ENST00000663543.1		n.290-37570C>T		intron	N/A
	LINC02542	ENST00000666226.1		n.121+6070C>T		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.281 AC: 42703 AN: 151900 Hom.: 6201 Cov.: 32

Gnomad AFR AF: 0.360

Gnomad AMI AF: 0.288

Gnomad AMR AF: 0.271

Gnomad ASJ AF: 0.240

Gnomad EAS AF: 0.200

Gnomad SAS AF: 0.334

Gnomad FIN AF: 0.219

Gnomad MID AF: 0.228

Gnomad NFE AF: 0.250

Gnomad OTH AF: 0.265

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

GnomAD4 genome AF: 0.281 AC: 42746 AN: 152018 Hom.: 6211 Cov.: 32 AF XY: 0.282 AC XY: 20959 AN XY: 74300

African (AFR) AF: 0.360 AC: 14937 AN: 41452

American (AMR) AF: 0.270 AC: 4130 AN: 15276

Ashkenazi Jewish (ASJ) AF: 0.240 AC: 834 AN: 3468

East Asian (EAS) AF: 0.200 AC: 1031 AN: 5154

South Asian (SAS) AF: 0.334 AC: 1606 AN: 4804

European-Finnish (FIN) AF: 0.219 AC: 2316 AN: 10566

Middle Eastern (MID) AF: 0.228 AC: 67 AN: 294

European-Non Finnish (NFE) AF: 0.250 AC: 17000 AN: 67978

Other (OTH) AF: 0.266 AC: 563 AN: 2116

Alfa AF: 0.259 Hom.: 8680

Bravo AF: 0.286

Asia WGS AF: 0.277 AC: 963 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	2.3
DANN	Benign	0.62
PhyloP100		-0.099

Splicing

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

Other links and lift over

dbSNP: rs1342196; hg19: chr6-82805292;