rs9436299

Variant names:

• chr1-65427205-C-A
• rs9436299
• NM_002303.6:c.-21+1827C>A

Your query was ambiguous. Multiple possible variants found:

• chr1-65427205-C-A
• chr1-65427205-C-T

Variant summary

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

The NM_002303.6(LEPR):​c.-21+1827C>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.693 in 152,060 control chromosomes in the GnomAD database, including 37,629 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 0.69 (37629 hom., cov: 32)
• Consequence: LEPR NM_002303.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.152
• Publications: 9 publications found

Genes affected

LEPR (HGNC:6554): (leptin receptor) The protein encoded by this gene belongs to the gp130 family of cytokine receptors that are known to stimulate gene transcription via activation of cytosolic STAT proteins. This protein is a receptor for leptin (an adipocyte-specific hormone that regulates body weight), and is involved in the regulation of fat metabolism, as well as in a novel hematopoietic pathway that is required for normal lymphopoiesis. Mutations in this gene have been associated with obesity and pituitary dysfunction. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. It is noteworthy that this gene and LEPROT gene (GeneID:54741) share the same promoter and the first 2 exons, however, encode distinct proteins (PMID:9207021).[provided by RefSeq, Nov 2010]

LEPROT (HGNC:29477): (leptin receptor overlapping transcript) LEPROT is associated with the Golgi complex and endosomes and has a role in cell surface expression of growth hormone receptor (GHR; MIM 600946) and leptin receptor (OBR, or LEPR; MIM 601007), thereby altering receptor-mediated cell signaling (Couturier et al., 2007 [PubMed 18042720]; Touvier et al., 2009 [PubMed 19907080]).[supplied by OMIM, Jul 2010]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.98).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.808 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_002303.6. 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
	LEPR	NM_002303.6	MANE Select	c.-21+1827C>A		intron	N/A	NP_002294.2
	LEPROT	NM_017526.5	MANE Select	c.92+1827C>A		intron	N/A	NP_059996.1	O15243
	LEPR	NM_001003680.3		c.-21+1827C>A		intron	N/A	NP_001003680.1	P48357-3

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	LEPR	ENST00000349533.11	TSL:1 MANE Select	c.-21+1827C>A		intron	N/A	ENSP00000330393.7	P48357-1
	LEPROT	ENST00000371065.9	TSL:1 MANE Select	c.92+1827C>A		intron	N/A	ENSP00000360104.4	O15243
	LEPR	ENST00000371059.7	TSL:1	c.-21+1827C>A		intron	N/A	ENSP00000360098.3	P48357-3

Frequencies

GnomAD3 genomes AF: 0.693 AC: 105333 AN: 151938 Hom.: 37604 Cov.: 32

Gnomad AFR AF: 0.815

Gnomad AMI AF: 0.679

Gnomad AMR AF: 0.676

Gnomad ASJ AF: 0.776

Gnomad EAS AF: 0.192

Gnomad SAS AF: 0.704

Gnomad FIN AF: 0.551

Gnomad MID AF: 0.801

Gnomad NFE AF: 0.677

Gnomad OTH AF: 0.701

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

GnomAD4 genome AF: 0.693 AC: 105410 AN: 152060 Hom.: 37629 Cov.: 32 AF XY: 0.684 AC XY: 50826 AN XY: 74302

African (AFR) AF: 0.815 AC: 33828 AN: 41492

American (AMR) AF: 0.675 AC: 10324 AN: 15286

Ashkenazi Jewish (ASJ) AF: 0.776 AC: 2691 AN: 3470

East Asian (EAS) AF: 0.192 AC: 992 AN: 5154

South Asian (SAS) AF: 0.703 AC: 3385 AN: 4814

European-Finnish (FIN) AF: 0.551 AC: 5810 AN: 10546

Middle Eastern (MID) AF: 0.796 AC: 234 AN: 294

European-Non Finnish (NFE) AF: 0.677 AC: 46047 AN: 67980

Other (OTH) AF: 0.701 AC: 1481 AN: 2114

Alfa AF: 0.662 Hom.: 5501

Bravo AF: 0.705

Asia WGS AF: 0.491 AC: 1710 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.98
CADD	Benign	0.97
DANN	Benign	0.55
PhyloP100		-0.15
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: rs9436299; hg19: chr1-65892888;