chr12-124848409-T-C

Variant names:

• chr12-124848409-T-C
• rs10773111
• NM_005505.5:c.126+15186A>G

Variant summary

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

The NM_005505.5(SCARB1):​c.126+15186A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.645 in 152,136 control chromosomes in the GnomAD database, including 32,035 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 0.64 (32035 hom., cov: 33)
• Consequence: SCARB1 NM_005505.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.68
• Publications: 21 publications found

Genes affected

SCARB1 (HGNC:1664): (scavenger receptor class B member 1) The protein encoded by this gene is a plasma membrane receptor for high density lipoprotein cholesterol (HDL). The encoded protein mediates cholesterol transfer to and from HDL. In addition, this protein is a receptor for hepatitis C virus glycoprotein E2 and facilitates cell entry by the virus, SARS-CoV2. [provided by RefSeq, Oct 2021]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.01).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.74 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_005505.5. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SCARB1	NM_005505.5	MANE Select	c.126+15186A>G		intron	N/A	NP_005496.4
	SCARB1	NM_001367981.1		c.126+15186A>G		intron	N/A	NP_001354910.1
	SCARB1	NM_001367983.1		c.126+15186A>G		intron	N/A	NP_001354912.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SCARB1	ENST00000261693.11	TSL:1 MANE Select	c.126+15186A>G		intron	N/A	ENSP00000261693.6
	SCARB1	ENST00000546215.5	TSL:1	c.126+15186A>G		intron	N/A	ENSP00000442862.1
	SCARB1	ENST00000535005.5	TSL:1	n.441+18580A>G		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.644 AC: 97955 AN: 152016 Hom.: 31973 Cov.: 33

Gnomad AFR AF: 0.747

Gnomad AMI AF: 0.608

Gnomad AMR AF: 0.660

Gnomad ASJ AF: 0.628

Gnomad EAS AF: 0.704

Gnomad SAS AF: 0.597

Gnomad FIN AF: 0.606

Gnomad MID AF: 0.622

Gnomad NFE AF: 0.584

Gnomad OTH AF: 0.657

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

GnomAD4 genome AF: 0.645 AC: 98081 AN: 152136 Hom.: 32035 Cov.: 33 AF XY: 0.647 AC XY: 48126 AN XY: 74382

African (AFR) AF: 0.747 AC: 31019 AN: 41516

American (AMR) AF: 0.660 AC: 10096 AN: 15298

Ashkenazi Jewish (ASJ) AF: 0.628 AC: 2179 AN: 3468

East Asian (EAS) AF: 0.704 AC: 3631 AN: 5160

South Asian (SAS) AF: 0.598 AC: 2889 AN: 4830

European-Finnish (FIN) AF: 0.606 AC: 6422 AN: 10592

Middle Eastern (MID) AF: 0.620 AC: 181 AN: 292

European-Non Finnish (NFE) AF: 0.584 AC: 39720 AN: 67958

Other (OTH) AF: 0.658 AC: 1392 AN: 2114

Alfa AF: 0.605 Hom.: 101710

Bravo AF: 0.654

Asia WGS AF: 0.702 AC: 2439 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	0.94
DANN	Benign	0.33
PhyloP100		-1.7
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: rs10773111; hg19: chr12-125332955;