2-118992035-C-T

Position:

• chr2-118992035-C-T

Variant summary

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

The NM_006770.4(MARCO):​c.1207+160C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.347 in 152,128 control chromosomes in the GnomAD database, including 10,622 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 0.35 (10622 hom., cov: 33)
• Consequence: MARCO NM_006770.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.759

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]

LOC124906072 (HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.88).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.462 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
MARCO	NM_006770.4	c.1207+160C>T		intron_variant		ENST00000327097.5	NP_006761.1
MARCO	XM_011512082.3	c.1207+160C>T		intron_variant			XP_011510384.1
MARCO	XM_011512083.4	c.844+160C>T		intron_variant			XP_011510385.1
LOC124906072	XR_007087213.1	n.249-869G>A		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
MARCO	ENST00000327097.5	c.1207+160C>T		intron_variant		1	NM_006770.4	ENSP00000318916.4

Frequencies

GnomAD3 genomes AF: 0.347 AC: 52803 AN: 152010 Hom.: 10619 Cov.: 33

Gnomad AFR AF: 0.142

Gnomad AMI AF: 0.270

Gnomad AMR AF: 0.342

Gnomad ASJ AF: 0.487

Gnomad EAS AF: 0.262

Gnomad SAS AF: 0.310

Gnomad FIN AF: 0.412

Gnomad MID AF: 0.364

Gnomad NFE AF: 0.466

Gnomad OTH AF: 0.377

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

GnomAD4 genome AF: 0.347 AC: 52816 AN: 152128 Hom.: 10622 Cov.: 33 AF XY: 0.344 AC XY: 25589 AN XY: 74372

Gnomad4 AFR AF: 0.142

Gnomad4 AMR AF: 0.341

Gnomad4 ASJ AF: 0.487

Gnomad4 EAS AF: 0.262

Gnomad4 SAS AF: 0.311

Gnomad4 FIN AF: 0.412

Gnomad4 NFE AF: 0.466

Gnomad4 OTH AF: 0.379

Alfa AF: 0.447 Hom.: 23826

Bravo AF: 0.337

Asia WGS AF: 0.312 AC: 1086 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.88
CADD	Benign	0.058
DANN	Benign	0.78

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.010		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: rs4848530; hg19: chr2-119749611; COSMIC: COSV59058375; COSMIC: COSV59058375;