rs533984

chr11-94466106-G-A

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_005591.4(MRE11):c.1098+1707C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.472 in 151,838 control chromosomes in the GnomAD database, including 17,955 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 0.47 (17955 hom., cov: 31)
• Consequence: MRE11 NM_005591.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.631

Genes affected

MRE11 (HGNC:7230): (MRE11 homolog, double strand break repair nuclease) This gene encodes a nuclear protein involved in homologous recombination, telomere length maintenance, and DNA double-strand break repair. By itself, the protein has 3' to 5' exonuclease activity and endonuclease activity. The protein forms a complex with the RAD50 homolog; this complex is required for nonhomologous joining of DNA ends and possesses increased single-stranded DNA endonuclease and 3' to 5' exonuclease activities. In conjunction with a DNA ligase, this protein promotes the joining of noncomplementary ends in vitro using short homologies near the ends of the DNA fragments. This gene has a pseudogene on chromosome 3. Alternative splicing of this gene results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.96).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.643 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
MRE11	NM_005591.4	c.1098+1707C>T		intron_variant		ENST00000323929.8

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
MRE11	ENST00000323929.8	c.1098+1707C>T		intron_variant		1	NM_005591.4	P3
MRE11	ENST00000323977.7	c.1098+1707C>T		intron_variant		1
MRE11	ENST00000393241.8	c.1098+1707C>T		intron_variant		5		A1
MRE11	ENST00000407439.7	c.1107+1707C>T		intron_variant		2

Frequencies

GnomAD3 genomes AF: 0.472 AC: 71582 AN: 151720 Hom.: 17938 Cov.: 31

Gnomad AFR AF: 0.649

Gnomad AMI AF: 0.0943

Gnomad AMR AF: 0.431

Gnomad ASJ AF: 0.389

Gnomad EAS AF: 0.459

Gnomad SAS AF: 0.564

Gnomad FIN AF: 0.391

Gnomad MID AF: 0.506

Gnomad NFE AF: 0.389

Gnomad OTH AF: 0.476

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

GnomAD4 genome AF: 0.472 AC: 71638 AN: 151838 Hom.: 17955 Cov.: 31 AF XY: 0.475 AC XY: 35211 AN XY: 74190

Gnomad4 AFR AF: 0.649

Gnomad4 AMR AF: 0.431

Gnomad4 ASJ AF: 0.389

Gnomad4 EAS AF: 0.458

Gnomad4 SAS AF: 0.566

Gnomad4 FIN AF: 0.391

Gnomad4 NFE AF: 0.389

Gnomad4 OTH AF: 0.471

Alfa AF: 0.413 Hom.: 13613

Bravo AF: 0.479

Asia WGS AF: 0.507 AC: 1763 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.96
Cadd	Benign	0.67
Dann	Benign	0.49

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

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

Publications

LitVar

Other links and lift over

dbSNP: rs533984; hg19: chr11-94199272;