rs2127565

Variant names:

• chr8-16129050-C-G
• rs2127565
• NM_138715.3:c.1034-8444G>C

Your query was ambiguous. Multiple possible variants found:

• chr8-16129050-C-G
• chr8-16129050-C-T

Variant summary

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

The NM_138715.3(MSR1):​c.1034-8444G>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.725 in 151,916 control chromosomes in the GnomAD database, including 42,871 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 0.73 (42871 hom., cov: 31)
• Consequence: MSR1 NM_138715.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0160
• Publications: 5 publications found

Genes affected

MSR1 (HGNC:7376): (macrophage scavenger receptor 1) This gene encodes the class A macrophage scavenger receptors, which include three different types (1, 2, 3) generated by alternative splicing of this gene. These receptors or isoforms are macrophage-specific trimeric integral membrane glycoproteins and have been implicated in many macrophage-associated physiological and pathological processes including atherosclerosis, Alzheimer's disease, and host defense. The isoforms type 1 and type 2 are functional receptors and are able to mediate the endocytosis of modified low density lipoproteins (LDLs). The isoform type 3 does not internalize modified LDL (acetyl-LDL) despite having the domain shown to mediate this function in the types 1 and 2 isoforms. It has an altered intracellular processing and is trapped within the endoplasmic reticulum, making it unable to perform endocytosis. The isoform type 3 can inhibit the function of isoforms type 1 and type 2 when co-expressed, indicating a dominant negative effect and suggesting a mechanism for regulation of scavenger receptor activity in macrophages. [provided by RefSeq, Jul 2008]

MSR1 Gene-Disease associations (from GenCC):

• Barrett esophagus

  Inheritance: Unknown Classification: LIMITED Submitted by: Laboratory for Molecular Medicine

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.87).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.866 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
MSR1	NM_138715.3	c.1034-8444G>C		intron_variant	Intron 8 of 9	ENST00000262101.10	NP_619729.1
MSR1	NM_001363744.1	c.1088-8444G>C		intron_variant	Intron 8 of 9		NP_001350673.1
MSR1	NM_138716.3	c.1033+14508G>C		intron_variant	Intron 8 of 8		NP_619730.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
MSR1	ENST00000262101.10	c.1034-8444G>C		intron_variant	Intron 8 of 9	1	NM_138715.3	ENSP00000262101.5

Frequencies

GnomAD3 genomes AF: 0.726 AC: 110165 AN: 151798 Hom.: 42859 Cov.: 31

Gnomad AFR AF: 0.422

Gnomad AMI AF: 0.886

Gnomad AMR AF: 0.726

Gnomad ASJ AF: 0.824

Gnomad EAS AF: 0.762

Gnomad SAS AF: 0.770

Gnomad FIN AF: 0.879

Gnomad MID AF: 0.782

Gnomad NFE AF: 0.872

Gnomad OTH AF: 0.763

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

GnomAD4 genome AF: 0.725 AC: 110192 AN: 151916 Hom.: 42871 Cov.: 31 AF XY: 0.726 AC XY: 53956 AN XY: 74282

African (AFR) AF: 0.421 AC: 17411 AN: 41354

American (AMR) AF: 0.726 AC: 11066 AN: 15250

Ashkenazi Jewish (ASJ) AF: 0.824 AC: 2860 AN: 3470

East Asian (EAS) AF: 0.762 AC: 3949 AN: 5180

South Asian (SAS) AF: 0.771 AC: 3710 AN: 4810

European-Finnish (FIN) AF: 0.879 AC: 9298 AN: 10580

Middle Eastern (MID) AF: 0.779 AC: 229 AN: 294

European-Non Finnish (NFE) AF: 0.872 AC: 59259 AN: 67966

Other (OTH) AF: 0.763 AC: 1604 AN: 2102

Alfa AF: 0.791 Hom.: 5900

Bravo AF: 0.699

Asia WGS AF: 0.750 AC: 2601 AN: 3468

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.87
CADD	Benign	2.0
DANN	Benign	0.59
PhyloP100		-0.016
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: rs2127565; hg19: chr8-15986559;