8-16120616-TAAAAAAAAAAAAAAAA-TAAAAAAAAAAAAAAAAAAAAAA

Variant names:

• chr8-16120616-T-TAAAAAA
• rs60866666
• NM_138715.3:c.1034-16_1034-11dupTTTTTT

Variant summary

Our verdict is Benign. The variant received -8 ACMG points: 0P and 8B. BS1 BS2

The NM_138715.3(MSR1):​c.1034-16_1034-11dupTTTTTT variant causes a intron change involving the alteration of a non-conserved nucleotide. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency:
  • Genomes: 𝑓 0.0084 (11 hom., cov: 0)
  • Exomes 𝑓: 0.0023 (6 hom.)
• Consequence: MSR1 NM_138715.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.140
• Publications: 0 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 -8 ACMG points.

• BS1: Variant frequency is greater than expected in population nfe. GnomAd4 allele frequency = 0.0084 (533/63462) while in subpopulation NFE AF = 0.0102 (358/35036). AF 95% confidence interval is 0.00935. There are 11 homozygotes in GnomAd4. There are 214 alleles in the male GnomAd4 subpopulation. Median coverage is 0. This position passed quality control check.
• BS2: High Homozygotes in GnomAd4 at 11 Unknown gene

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_138715.3. 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
	MSR1	NM_138715.3	MANE Select	c.1034-16_1034-11dupTTTTTT		intron	N/A	NP_619729.1	P21757-1
	MSR1	NM_001363744.1		c.1088-16_1088-11dupTTTTTT		intron	N/A	NP_001350673.1	B4DDJ5
	MSR1	NM_138716.3		c.1034-10404_1034-10399dupTTTTTT		intron	N/A	NP_619730.1	P21757-3

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	MSR1	ENST00000262101.10	TSL:1 MANE Select	c.1034-11_1034-10insTTTTTT		intron	N/A	ENSP00000262101.5	P21757-1
	MSR1	ENST00000445506.6	TSL:1	c.1088-11_1088-10insTTTTTT		intron	N/A	ENSP00000405453.2	B4DDJ5
	MSR1	ENST00000355282.6	TSL:1	c.1034-10399_1034-10398insTTTTTT		intron	N/A	ENSP00000347430.2	P21757-3

Frequencies

GnomAD3 genomes AF: 0.00840 AC: 533 AN: 63460 Hom.: 11 Cov.: 0

Gnomad AFR AF: 0.00706

Gnomad AMI AF: 0.00405

Gnomad AMR AF: 0.00529

Gnomad ASJ AF: 0.00956

Gnomad EAS AF: 0.00384

Gnomad SAS AF: 0.000664

Gnomad FIN AF: 0.00213

Gnomad MID AF: 0.00

Gnomad NFE AF: 0.0102

Gnomad OTH AF: 0.00656

GnomAD4 exome AF: 0.00227 AC: 2566 AN: 1132450 Hom.: 6 Cov.: 0 AF XY: 0.00229 AC XY: 1283 AN XY: 560508

⚠️ The allele balance in gnomAD version 4 Exomes is significantly skewed from the expected value of 0.5.

African (AFR) AF: 0.00281 AC: 63 AN: 22402

American (AMR) AF: 0.00562 AC: 125 AN: 22238

Ashkenazi Jewish (ASJ) AF: 0.00261 AC: 51 AN: 19534

East Asian (EAS) AF: 0.00310 AC: 86 AN: 27768

South Asian (SAS) AF: 0.00207 AC: 125 AN: 60384

European-Finnish (FIN) AF: 0.00187 AC: 49 AN: 26250

Middle Eastern (MID) AF: 0.00164 AC: 5 AN: 3042

European-Non Finnish (NFE) AF: 0.00215 AC: 1941 AN: 904888

Other (OTH) AF: 0.00263 AC: 121 AN: 45944

⚠️ The allele balance in gnomAD4 Exomes is highly skewed from 0.5 (p-value = 0), which strongly suggests a high chance of mosaicism in these individuals.

GnomAD4 genome AF: 0.00840 AC: 533 AN: 63462 Hom.: 11 Cov.: 0 AF XY: 0.00750 AC XY: 214 AN XY: 28548

African (AFR) AF: 0.00705 AC: 116 AN: 16454

American (AMR) AF: 0.00529 AC: 22 AN: 4156

Ashkenazi Jewish (ASJ) AF: 0.00956 AC: 19 AN: 1988

East Asian (EAS) AF: 0.00384 AC: 8 AN: 2082

South Asian (SAS) AF: 0.000671 AC: 1 AN: 1490

European-Finnish (FIN) AF: 0.00213 AC: 2 AN: 938

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 58

European-Non Finnish (NFE) AF: 0.0102 AC: 358 AN: 35036

Other (OTH) AF: 0.00653 AC: 5 AN: 766

Alfa AF: 0.00 Hom.: 0

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
PhyloP100		0.14

Splicing

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

Other links and lift over

dbSNP: rs60866666; hg19: chr8-15978125;