rs10824793

chr10-52769720-G-A

Variant summary

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

The NM_001378373.1(MBL2):c.305-405C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.492 in 152,010 control chromosomes in the GnomAD database, including 19,972 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 0.49 (19972 hom., cov: 32)
• Consequence: MBL2 NM_001378373.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.493

Genes affected

MBL2 (HGNC:6922): (mannose binding lectin 2) This gene encodes the soluble mannose-binding lectin or mannose-binding protein found in serum. The protein encoded belongs to the collectin family and is an important element in the innate immune system. The protein recognizes and binds to mannose and N-acetylglucosamine on many microorganisms, including bacteria, yeast, and viruses including influenza virus, HIV and SARS-CoV. This binding activates the classical complement pathway. Deficiencies of this gene have been associated with susceptibility to autoimmune and infectious diseases. [provided by RefSeq, Jun 2020]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.86).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.629 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
MBL2	NM_001378373.1	c.305-405C>T		intron_variant		ENST00000674931.1
MBL2	NM_000242.3	c.305-405C>T		intron_variant
MBL2	NM_001378374.1	c.305-405C>T		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
MBL2	ENST00000674931.1	c.305-405C>T		intron_variant			NM_001378373.1	P1
MBL2	ENST00000373968.3	c.305-405C>T		intron_variant		1		P1
MBL2	ENST00000675947.1	c.305-405C>T		intron_variant				P1

Frequencies

GnomAD3 genomes AF: 0.492 AC: 74754 AN: 151892 Hom.: 19949 Cov.: 32

Gnomad AFR AF: 0.266

Gnomad AMI AF: 0.747

Gnomad AMR AF: 0.625

Gnomad ASJ AF: 0.579

Gnomad EAS AF: 0.647

Gnomad SAS AF: 0.494

Gnomad FIN AF: 0.618

Gnomad MID AF: 0.490

Gnomad NFE AF: 0.560

Gnomad OTH AF: 0.512

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

GnomAD4 genome AF: 0.492 AC: 74803 AN: 152010 Hom.: 19972 Cov.: 32 AF XY: 0.499 AC XY: 37075 AN XY: 74310

Gnomad4 AFR AF: 0.266

Gnomad4 AMR AF: 0.625

Gnomad4 ASJ AF: 0.579

Gnomad4 EAS AF: 0.648

Gnomad4 SAS AF: 0.493

Gnomad4 FIN AF: 0.618

Gnomad4 NFE AF: 0.560

Gnomad4 OTH AF: 0.518

Alfa AF: 0.533 Hom.: 4835

Bravo AF: 0.488

Asia WGS AF: 0.592 AC: 2058 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.86
Cadd	Benign	0.78
Dann	Benign	0.73

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: rs10824793; hg19: chr10-54529480;