11-47257366-C-T

Position:

• chr11-47257366-C-T

Variant summary

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

The NM_001251934.2(NR1H3):​c.62-2425C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.378 in 151,982 control chromosomes in the GnomAD database, including 11,795 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 0.38 (11795 hom., cov: 31)
• Consequence: NR1H3 NM_001251934.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.23

Genes affected

NR1H3 (HGNC:7966): (nuclear receptor subfamily 1 group H member 3) The protein encoded by this gene belongs to the NR1 subfamily of the nuclear receptor superfamily. The NR1 family members are key regulators of macrophage function, controlling transcriptional programs involved in lipid homeostasis and inflammation. This protein is highly expressed in visceral organs, including liver, kidney and intestine. It forms a heterodimer with retinoid X receptor (RXR), and regulates expression of target genes containing retinoid response elements. Studies in mice lacking this gene suggest that it may play an important role in the regulation of cholesterol homeostasis. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]

NR1H3 (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 (EAS) allele frequency at 95% confidence interval = 0.726 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
NR1H3	NM_001251934.2	c.62-2425C>T		intron_variant			NP_001238863.1
NR1H3	NM_001251935.2	c.62-2425C>T		intron_variant			NP_001238864.1
NR1H3	NM_001130102.3	c.-92-2425C>T		intron_variant			NP_001123574.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
NR1H3	ENST00000616973.4	c.62-2425C>T		intron_variant		1		ENSP00000477707.1
NR1H3	ENST00000395397.7	c.-92-2425C>T		intron_variant		1		ENSP00000378793.3
NR1H3	ENST00000527464.5	n.283-2425C>T		intron_variant		1

Frequencies

GnomAD3 genomes AF: 0.378 AC: 57380 AN: 151864 Hom.: 11796 Cov.: 31

Gnomad AFR AF: 0.471

Gnomad AMI AF: 0.133

Gnomad AMR AF: 0.353

Gnomad ASJ AF: 0.224

Gnomad EAS AF: 0.745

Gnomad SAS AF: 0.465

Gnomad FIN AF: 0.427

Gnomad MID AF: 0.248

Gnomad NFE AF: 0.298

Gnomad OTH AF: 0.327

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

GnomAD4 genome AF: 0.378 AC: 57402 AN: 151982 Hom.: 11795 Cov.: 31 AF XY: 0.388 AC XY: 28809 AN XY: 74270

Gnomad4 AFR AF: 0.471

Gnomad4 AMR AF: 0.353

Gnomad4 ASJ AF: 0.224

Gnomad4 EAS AF: 0.746

Gnomad4 SAS AF: 0.465

Gnomad4 FIN AF: 0.427

Gnomad4 NFE AF: 0.298

Gnomad4 OTH AF: 0.323

Alfa AF: 0.293 Hom.: 4147

Bravo AF: 0.375

Asia WGS AF: 0.543 AC: 1884 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	0.043
DANN	Benign	0.48

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs3758673; hg19: chr11-47278917;