ENST00000452813.1:n.394+7964A>G

Variant names:

• chr2-217310749-A-G
• rs4141835
• ENST00000452813.1:n.394+7964A>G

Variant summary

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

The ENST00000452813.1(TESHL):​n.394+7964A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.736 in 152,140 control chromosomes in the GnomAD database, including 41,644 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 0.74 (41644 hom., cov: 33)
• Consequence: TESHL ENST00000452813.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.887
• Publications: 5 publications found

Genes affected

TESHL (HGNC:52740): (testicular germ cell expressed HSF2 interacting lncRNA)

DIRC3 (HGNC:17805): (disrupted in renal carcinoma 3)

DIRC3-AS1 (HGNC:50636): (DIRC3 antisense RNA 1)

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.92).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.769 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000452813.1. 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
	DIRC3	NR_026597.2		n.3065+7217T>C		intron	N/A
	DIRC3-AS1	NR_133642.1		n.400+7964A>G		intron	N/A
	DIRC3	NR_186292.1		n.4304+7217T>C		intron	N/A

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	TESHL	ENST00000452813.1	TSL:3	n.394+7964A>G		intron	N/A
	DIRC3	ENST00000474063.5	TSL:2	n.2233+7217T>C		intron	N/A
	DIRC3	ENST00000486365.6	TSL:5	n.3065+7217T>C		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.737 AC: 111987 AN: 152022 Hom.: 41622 Cov.: 33

Gnomad AFR AF: 0.660

Gnomad AMI AF: 0.810

Gnomad AMR AF: 0.723

Gnomad ASJ AF: 0.834

Gnomad EAS AF: 0.732

Gnomad SAS AF: 0.676

Gnomad FIN AF: 0.804

Gnomad MID AF: 0.759

Gnomad NFE AF: 0.774

Gnomad OTH AF: 0.742

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

GnomAD4 genome AF: 0.736 AC: 112051 AN: 152140 Hom.: 41644 Cov.: 33 AF XY: 0.738 AC XY: 54859 AN XY: 74384

African (AFR) AF: 0.660 AC: 27361 AN: 41486

American (AMR) AF: 0.723 AC: 11063 AN: 15294

Ashkenazi Jewish (ASJ) AF: 0.834 AC: 2895 AN: 3472

East Asian (EAS) AF: 0.731 AC: 3780 AN: 5168

South Asian (SAS) AF: 0.674 AC: 3249 AN: 4818

European-Finnish (FIN) AF: 0.804 AC: 8516 AN: 10594

Middle Eastern (MID) AF: 0.765 AC: 225 AN: 294

European-Non Finnish (NFE) AF: 0.774 AC: 52656 AN: 67990

Other (OTH) AF: 0.742 AC: 1567 AN: 2112

Alfa AF: 0.760 Hom.: 185677

Bravo AF: 0.724

Asia WGS AF: 0.685 AC: 2384 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.92
CADD	Benign	0.091
DANN	Benign	0.32
PhyloP100		-0.89

Splicing

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

Other links and lift over

dbSNP: rs4141835; hg19: chr2-218175472;