13-54180396-T-C

Variant names:

• chr13-54180396-T-C
• rs632059
• ENST00000706980.1:n.120-52967A>G

Variant summary

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

The ENST00000706980.1(LINC00458):​n.120-52967A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.965 in 152,208 control chromosomes in the GnomAD database, including 70,906 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 0.96 (70906 hom., cov: 31)
• Consequence: LINC00458 ENST00000706980.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.376
• Publications: 0 publications found

Genes affected

LINC00458 (HGNC:42807): (long intergenic non-protein coding RNA 458)

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.88).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.968 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000706980.1. 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
There are no transcript annotations for this variant.

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	LINC00458	ENST00000706980.1		n.120-52967A>G		intron	N/A
	LINC00458	ENST00000706981.1		n.200-52967A>G		intron	N/A
	LINC00458	ENST00000706986.1		n.110+2988A>G		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.965 AC: 146771 AN: 152090 Hom.: 70857 Cov.: 31

Gnomad AFR AF: 0.952

Gnomad AMI AF: 0.988

Gnomad AMR AF: 0.972

Gnomad ASJ AF: 0.974

Gnomad EAS AF: 0.893

Gnomad SAS AF: 0.991

Gnomad FIN AF: 0.975

Gnomad MID AF: 1.00

Gnomad NFE AF: 0.972

Gnomad OTH AF: 0.967

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

GnomAD4 genome AF: 0.965 AC: 146878 AN: 152208 Hom.: 70906 Cov.: 31 AF XY: 0.965 AC XY: 71819 AN XY: 74408

African (AFR) AF: 0.952 AC: 39536 AN: 41516

American (AMR) AF: 0.973 AC: 14868 AN: 15288

Ashkenazi Jewish (ASJ) AF: 0.974 AC: 3382 AN: 3472

East Asian (EAS) AF: 0.893 AC: 4596 AN: 5148

South Asian (SAS) AF: 0.991 AC: 4773 AN: 4816

European-Finnish (FIN) AF: 0.975 AC: 10357 AN: 10622

Middle Eastern (MID) AF: 1.00 AC: 294 AN: 294

European-Non Finnish (NFE) AF: 0.972 AC: 66130 AN: 68026

Other (OTH) AF: 0.965 AC: 2041 AN: 2114

Alfa AF: 0.969 Hom.: 8690

Bravo AF: 0.963

Asia WGS AF: 0.954 AC: 3315 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.88
CADD	Benign	0.97
DANN	Benign	0.76
PhyloP100		-0.38

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: rs632059;

hg19: chr13-54754531;