2-11668738-C-T

Variant names:

• chr2-11668738-C-T
• rs4669767
• NM_012344.4:c.624+768G>A

Variant summary

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

The NM_012344.4(NTSR2):​c.624+768G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.447 in 152,018 control chromosomes in the GnomAD database, including 16,477 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 0.45 (16477 hom., cov: 33)
• Consequence: NTSR2 NM_012344.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -2.68
• Publications: 2 publications found

Genes affected

NTSR2 (HGNC:8040): (neurotensin receptor 2) The protein encoded by this gene belongs to the G protein-coupled receptor family that activate a phosphatidylinositol-calcium second messenger system. Binding and pharmacological studies demonstrate that this receptor binds neurotensin as well as several other ligands already described for neurotensin NT1 receptor. However, unlike NT1 receptor, this gene recognizes, with high affinity, levocabastine, a histamine H1 receptor antagonist previously shown to compete with neurotensin for low-affinity binding sites in brain. These activities suggest that this receptor may be of physiological importance and that a natural agonist for the receptor may exist. [provided by RefSeq, Jul 2008]

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 (SAS) allele frequency at 95% confidence interval = 0.601 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
NTSR2	NM_012344.4	c.624+768G>A		intron_variant	Intron 1 of 3	ENST00000306928.6	NP_036476.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
NTSR2	ENST00000306928.6	c.624+768G>A		intron_variant	Intron 1 of 3	1	NM_012344.4	ENSP00000303686.5

Frequencies

GnomAD3 genomes AF: 0.448 AC: 68027 AN: 151900 Hom.: 16488 Cov.: 33

Gnomad AFR AF: 0.252

Gnomad AMI AF: 0.575

Gnomad AMR AF: 0.535

Gnomad ASJ AF: 0.553

Gnomad EAS AF: 0.342

Gnomad SAS AF: 0.620

Gnomad FIN AF: 0.502

Gnomad MID AF: 0.427

Gnomad NFE AF: 0.527

Gnomad OTH AF: 0.473

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

GnomAD4 genome AF: 0.447 AC: 68024 AN: 152018 Hom.: 16477 Cov.: 33 AF XY: 0.450 AC XY: 33447 AN XY: 74294

African (AFR) AF: 0.252 AC: 10435 AN: 41470

American (AMR) AF: 0.535 AC: 8179 AN: 15288

Ashkenazi Jewish (ASJ) AF: 0.553 AC: 1920 AN: 3470

East Asian (EAS) AF: 0.341 AC: 1759 AN: 5154

South Asian (SAS) AF: 0.619 AC: 2984 AN: 4820

European-Finnish (FIN) AF: 0.502 AC: 5283 AN: 10534

Middle Eastern (MID) AF: 0.421 AC: 123 AN: 292

European-Non Finnish (NFE) AF: 0.527 AC: 35821 AN: 67974

Other (OTH) AF: 0.473 AC: 997 AN: 2106

Alfa AF: 0.448 Hom.: 5886

Bravo AF: 0.437

Asia WGS AF: 0.503 AC: 1748 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.98
CADD	Benign	1.1
DANN	Benign	0.42
PhyloP100		-2.7
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: rs4669767; hg19: chr2-11808864; COSMIC: COSV60993055; COSMIC: COSV60993055;