ENST00000752769.1:n.742_748dupTTTTTTT

Variant names:

• chr2-28391866-C-CTTTTTTT
• rs4042624
• ENST00000752769.1:n.742_748dupTTTTTTT

Variant summary

Our verdict is Benign. The variant received -8 ACMG points: 0P and 8B. BS1 BS2

The ENST00000752769.1(ENSG00000298060):​n.742_748dupTTTTTTT variant causes a non coding transcript exon change involving the alteration of a non-conserved nucleotide. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.018 (45 hom., cov: 0)
• Consequence: ENSG00000298060 ENST00000752769.1 non_coding_transcript_exon
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.161
• Publications: 1 publications found

Genes affected

ENSG00000298060 (HGNC:):

FOSL2-AS1 (HGNC:55784): (FOSL2 antisense RNA 1)

ACMG classification

Our verdict: Benign. The variant received -8 ACMG points.

• BS1: Variant frequency is greater than expected in population sas. GnomAd4 allele frequency = 0.0177 (2226/125480) while in subpopulation SAS AF = 0.0515 (190/3692). AF 95% confidence interval is 0.0455. There are 45 homozygotes in GnomAd4. There are 1041 alleles in the male GnomAd4 subpopulation. Median coverage is 0. This position passed quality control check.
• BS2: High Homozygotes in GnomAd4 at 45 gene

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000752769.1. 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
	FOSL2-AS1	NR_103831.1		n.125+2675_125+2681dupAAAAAAA		intron	N/A

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ENSG00000298060	ENST00000752769.1		n.742_748dupTTTTTTT		non_coding_transcript_exon	Exon 2 of 2
	ENSG00000298060	ENST00000752770.1		n.362_368dupTTTTTTT		non_coding_transcript_exon	Exon 2 of 2
	FOSL2-AS1	ENST00000427929.5	TSL:2	n.125+2675_125+2681dupAAAAAAA		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.0177 AC: 2227 AN: 125486 Hom.: 45 Cov.: 0

Gnomad AFR AF: 0.00409

Gnomad AMI AF: 0.0224

Gnomad AMR AF: 0.0142

Gnomad ASJ AF: 0.0170

Gnomad EAS AF: 0.000445

Gnomad SAS AF: 0.0517

Gnomad FIN AF: 0.00431

Gnomad MID AF: 0.00439

Gnomad NFE AF: 0.0260

Gnomad OTH AF: 0.0206

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

GnomAD4 genome AF: 0.0177 AC: 2226 AN: 125480 Hom.: 45 Cov.: 0 AF XY: 0.0176 AC XY: 1041 AN XY: 59148

African (AFR) AF: 0.00409 AC: 133 AN: 32546

American (AMR) AF: 0.0142 AC: 179 AN: 12586

Ashkenazi Jewish (ASJ) AF: 0.0170 AC: 55 AN: 3234

East Asian (EAS) AF: 0.000446 AC: 2 AN: 4488

South Asian (SAS) AF: 0.0515 AC: 190 AN: 3692

European-Finnish (FIN) AF: 0.00431 AC: 21 AN: 4876

Middle Eastern (MID) AF: 0.00481 AC: 1 AN: 208

European-Non Finnish (NFE) AF: 0.0260 AC: 1591 AN: 61292

Other (OTH) AF: 0.0205 AC: 35 AN: 1708

Alfa AF: 0.00909 Hom.: 206

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
PhyloP100		-0.16
Mutation Taster		=100/0	polymorphism

Splicing

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

Other links and lift over

dbSNP: rs4042624; hg19: chr2-28614733;