rs3846318

Positions:

• chr4-148244236-G-A
• chr4-148244236-G-C

Variant summary

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

The NM_000901.5(NR3C2):​c.1897+15742C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.647 in 152,070 control chromosomes in the GnomAD database, including 32,285 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 0.65 (32285 hom., cov: 32)
• Consequence: NR3C2 NM_000901.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.141

Genes affected

NR3C2 (HGNC:7979): (nuclear receptor subfamily 3 group C member 2) This gene encodes the mineralocorticoid receptor, which mediates aldosterone actions on salt and water balance within restricted target cells. The protein functions as a ligand-dependent transcription factor that binds to mineralocorticoid response elements in order to transactivate target genes. Mutations in this gene cause autosomal dominant pseudohypoaldosteronism type I, a disorder characterized by urinary salt wasting. Defects in this gene are also associated with early onset hypertension with severe exacerbation in pregnancy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.97).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.833 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
NR3C2	NM_000901.5	c.1897+15742C>T		intron_variant		ENST00000358102.8	NP_000892.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
NR3C2	ENST00000358102.8	c.1897+15742C>T		intron_variant		1	NM_000901.5	ENSP00000350815.3

Frequencies

GnomAD3 genomes AF: 0.647 AC: 98328 AN: 151952 Hom.: 32234 Cov.: 32

Gnomad AFR AF: 0.727

Gnomad AMI AF: 0.668

Gnomad AMR AF: 0.693

Gnomad ASJ AF: 0.580

Gnomad EAS AF: 0.855

Gnomad SAS AF: 0.651

Gnomad FIN AF: 0.591

Gnomad MID AF: 0.509

Gnomad NFE AF: 0.585

Gnomad OTH AF: 0.642

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

GnomAD4 genome AF: 0.647 AC: 98440 AN: 152070 Hom.: 32285 Cov.: 32 AF XY: 0.651 AC XY: 48396 AN XY: 74304

Gnomad4 AFR AF: 0.727

Gnomad4 AMR AF: 0.693

Gnomad4 ASJ AF: 0.580

Gnomad4 EAS AF: 0.854

Gnomad4 SAS AF: 0.651

Gnomad4 FIN AF: 0.591

Gnomad4 NFE AF: 0.585

Gnomad4 OTH AF: 0.645

Alfa AF: 0.594 Hom.: 35692

Bravo AF: 0.658

Asia WGS AF: 0.755 AC: 2619 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.97
CADD	Benign	2.6
DANN	Benign	0.40

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

Publications

LitVar

Other links and lift over

dbSNP: rs3846318; hg19: chr4-149165388;