rs10455657

Variant names:

• chr6-68275038-T-G
• rs10455657
• ENST00000445346.1:n.238-8423A>C

Variant summary

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

The ENST00000445346.1(LINC02549):​n.238-8423A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.231 in 151,906 control chromosomes in the GnomAD database, including 4,811 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 0.23 (4811 hom., cov: 32)
• Consequence: LINC02549 ENST00000445346.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.694
• Publications: 9 publications found

Genes affected

LINC02549 (HGNC:53584): (long intergenic non-protein coding RNA 2549)

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.379 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000445346.1. 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
	LINC02549	NR_125854.1		n.238-8423A>C		intron	N/A

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	LINC02549	ENST00000445346.1	TSL:1	n.238-8423A>C		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.230 AC: 34982 AN: 151788 Hom.: 4796 Cov.: 32

Gnomad AFR AF: 0.384

Gnomad AMI AF: 0.143

Gnomad AMR AF: 0.148

Gnomad ASJ AF: 0.219

Gnomad EAS AF: 0.00270

Gnomad SAS AF: 0.139

Gnomad FIN AF: 0.162

Gnomad MID AF: 0.171

Gnomad NFE AF: 0.194

Gnomad OTH AF: 0.191

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

GnomAD4 genome AF: 0.231 AC: 35017 AN: 151906 Hom.: 4811 Cov.: 32 AF XY: 0.226 AC XY: 16766 AN XY: 74220

African (AFR) AF: 0.384 AC: 15892 AN: 41438

American (AMR) AF: 0.147 AC: 2246 AN: 15248

Ashkenazi Jewish (ASJ) AF: 0.219 AC: 758 AN: 3468

East Asian (EAS) AF: 0.00270 AC: 14 AN: 5182

South Asian (SAS) AF: 0.139 AC: 670 AN: 4822

European-Finnish (FIN) AF: 0.162 AC: 1707 AN: 10546

Middle Eastern (MID) AF: 0.160 AC: 47 AN: 294

European-Non Finnish (NFE) AF: 0.194 AC: 13155 AN: 67888

Other (OTH) AF: 0.189 AC: 398 AN: 2108

Alfa AF: 0.205 Hom.: 9895

Bravo AF: 0.234

Asia WGS AF: 0.0850 AC: 297 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	8.4
DANN	Benign	0.52
PhyloP100		0.69

Splicing

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

MaxEntScan Visualizer can be used to analyze the impact of this mutation on the neighboring sequence.

Other links and lift over

dbSNP: rs10455657;

hg19: chr6-68984930;