rs34532313

Variant names:

• chr4-186539336-C-T
• rs34532313
• NM_005958.4:c.185-4779G>A

Variant summary

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

The NM_005958.4(MTNR1A):​c.185-4779G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.211 in 151,746 control chromosomes in the GnomAD database, including 4,014 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 0.21 (4014 hom., cov: 31)
• Consequence: MTNR1A NM_005958.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.140
• Publications: 4 publications found

Genes affected

MTNR1A (HGNC:7463): (melatonin receptor 1A) This gene encodes one of two high affinity forms of a receptor for melatonin, the primary hormone secreted by the pineal gland. This receptor is a G-protein coupled, 7-transmembrane receptor that is responsible for melatonin effects on mammalian circadian rhythm and reproductive alterations affected by day length. The receptor is an integral membrane protein that is readily detectable and localized to two specific regions of the brain. The hypothalamic suprachiasmatic nucleus appears to be involved in circadian rhythm while the hypophysial pars tuberalis may be responsible for the reproductive effects of melatonin. [provided by RefSeq, Jul 2008]

ENSG00000272297 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.56 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
MTNR1A	NM_005958.4	c.185-4779G>A		intron_variant	Intron 1 of 1	ENST00000307161.5	NP_005949.1
LOC105377596	XR_007058498.1	n.144-6308C>T		intron_variant	Intron 2 of 2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
MTNR1A	ENST00000307161.5	c.185-4779G>A		intron_variant	Intron 1 of 1	1	NM_005958.4	ENSP00000302811.5
ENSG00000272297	ENST00000509111.2	c.145+15846G>A		intron_variant	Intron 1 of 1	3		ENSP00000422449.2

Frequencies

GnomAD3 genomes AF: 0.211 AC: 31957 AN: 151628 Hom.: 4015 Cov.: 31

Gnomad AFR AF: 0.222

Gnomad AMI AF: 0.331

Gnomad AMR AF: 0.244

Gnomad ASJ AF: 0.153

Gnomad EAS AF: 0.577

Gnomad SAS AF: 0.444

Gnomad FIN AF: 0.181

Gnomad MID AF: 0.127

Gnomad NFE AF: 0.159

Gnomad OTH AF: 0.179

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

GnomAD4 genome AF: 0.211 AC: 31984 AN: 151746 Hom.: 4014 Cov.: 31 AF XY: 0.218 AC XY: 16137 AN XY: 74168

African (AFR) AF: 0.222 AC: 9162 AN: 41328

American (AMR) AF: 0.245 AC: 3745 AN: 15256

Ashkenazi Jewish (ASJ) AF: 0.153 AC: 528 AN: 3462

East Asian (EAS) AF: 0.577 AC: 2965 AN: 5140

South Asian (SAS) AF: 0.444 AC: 2132 AN: 4806

European-Finnish (FIN) AF: 0.181 AC: 1905 AN: 10508

Middle Eastern (MID) AF: 0.133 AC: 39 AN: 294

European-Non Finnish (NFE) AF: 0.159 AC: 10828 AN: 67928

Other (OTH) AF: 0.179 AC: 378 AN: 2112

Alfa AF: 0.201 Hom.: 1278

Bravo AF: 0.216

Asia WGS AF: 0.459 AC: 1592 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	5.8
DANN	Benign	0.67
PhyloP100		-0.14
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: rs34532313; hg19: chr4-187460490;