rs6752783

Variant names:

• chr2-118948829-T-G
• rs6752783
• NM_006770.4:c.97+6432T>G

Variant summary

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

The NM_006770.4(MARCO):​c.97+6432T>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.223 in 151,970 control chromosomes in the GnomAD database, including 5,732 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 0.22 (5732 hom., cov: 33)
• Consequence: MARCO NM_006770.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.879
• Publications: 4 publications found

Genes affected

MARCO (HGNC:6895): (macrophage receptor with collagenous structure) The protein encoded by this gene is a member of the class A scavenger receptor family and is part of the innate antimicrobial immune system. The protein may bind both Gram-negative and Gram-positive bacteria via an extracellular, C-terminal, scavenger receptor cysteine-rich (SRCR) domain. In addition to short cytoplasmic and transmembrane domains, there is an extracellular spacer domain and a long, extracellular collagenous domain. The protein may form a trimeric molecule by the association of the collagenous domains of three identical polypeptide chains. [provided by RefSeq, Jul 2008]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.02).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.464 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_006770.4. 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
	MARCO	NM_006770.4	MANE Select	c.97+6432T>G		intron	N/A	NP_006761.1	Q4ZG40

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	MARCO	ENST00000327097.5	TSL:1 MANE Select	c.97+6432T>G		intron	N/A	ENSP00000318916.4	Q9UEW3-1
	MARCO	ENST00000874357.1		c.97+6432T>G		intron	N/A	ENSP00000544416.1
	MARCO	ENST00000958830.1		c.97+6432T>G		intron	N/A	ENSP00000628889.1

Frequencies

GnomAD3 genomes AF: 0.223 AC: 33918 AN: 151852 Hom.: 5725 Cov.: 33

Gnomad AFR AF: 0.470

Gnomad AMI AF: 0.104

Gnomad AMR AF: 0.116

Gnomad ASJ AF: 0.112

Gnomad EAS AF: 0.220

Gnomad SAS AF: 0.307

Gnomad FIN AF: 0.155

Gnomad MID AF: 0.155

Gnomad NFE AF: 0.112

Gnomad OTH AF: 0.187

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

GnomAD4 genome AF: 0.223 AC: 33958 AN: 151970 Hom.: 5732 Cov.: 33 AF XY: 0.226 AC XY: 16765 AN XY: 74320

African (AFR) AF: 0.470 AC: 19411 AN: 41332

American (AMR) AF: 0.116 AC: 1769 AN: 15292

Ashkenazi Jewish (ASJ) AF: 0.112 AC: 390 AN: 3468

East Asian (EAS) AF: 0.220 AC: 1138 AN: 5172

South Asian (SAS) AF: 0.306 AC: 1473 AN: 4810

European-Finnish (FIN) AF: 0.155 AC: 1640 AN: 10592

Middle Eastern (MID) AF: 0.156 AC: 46 AN: 294

European-Non Finnish (NFE) AF: 0.112 AC: 7597 AN: 67992

Other (OTH) AF: 0.190 AC: 400 AN: 2110

Alfa AF: 0.156 Hom.: 892

Bravo AF: 0.228

Asia WGS AF: 0.236 AC: 819 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	0.64
DANN	Benign	0.33
PhyloP100		-0.88
Mutation Taster		=100/0	polymorphism (auto)

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

Other links and lift over

dbSNP: rs6752783; hg19: chr2-119706405;