rs764264847

Variant names:

• chr2-215944948-C-A
• rs764264847
• NM_018000.3:c.560G>T

Your query was ambiguous. Multiple possible variants found:

• chr2-215944948-C-A
• chr2-215944948-C-G
• chr2-215944948-C-T

Variant summary

Our verdict is Uncertain significance. Variant got 0 ACMG points: 2P and 2B. PM2 BP4_Moderate

The NM_018000.3(MREG):​c.560G>T​(p.Arg187Leu) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. 13/21 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar. Another variant affecting the same amino acid position, but resulting in a different missense (i.e. R187H) has been classified as Uncertain significance.

• Frequency: Genomes: not found (cov: 31)
• Consequence: MREG NM_018000.3 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.79

Genes affected

MREG (HGNC:25478): (melanoregulin) Predicted to enable phosphatidylinositol binding activity. Predicted to be involved in melanocyte differentiation; melanosome transport; and phagosome maturation. Predicted to act upstream of or within developmental pigmentation. Predicted to be located in late endosome membrane and melanosome membrane. Predicted to be intrinsic component of organelle membrane. Predicted to be part of protein-containing complex. Predicted to be active in melanosome. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Verdict is Uncertain_significance. Variant got 0 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.1631799).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
MREG	NM_018000.3	c.560G>T	p.Arg187Leu	missense_variant	Exon 5 of 5	ENST00000263268.11	NP_060470.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
MREG	ENST00000263268.11	c.560G>T	p.Arg187Leu	missense_variant	Exon 5 of 5	2	NM_018000.3	ENSP00000263268.6
MREG	ENST00000439791.5	c.*11G>T		downstream_gene_variant		4		ENSP00000411076.1
MREG	ENST00000424992.5	c.*40G>T		downstream_gene_variant		5		ENSP00000413302.1

Frequencies

GnomAD3 genomes Cov.: 31

GnomAD4 exome Cov.: 30

GnomAD4 genome Cov.: 31

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.13
BayesDel_addAF	Benign	-0.17	T
BayesDel_noAF	Benign	-0.48
CADD	Benign	20
DANN	Uncertain	0.99
DEOGEN2	Uncertain	0.47	T;T
Eigen	Benign	-0.19
Eigen_PC	Benign	0.010
FATHMM_MKL	Uncertain	0.88	D
LIST_S2	Uncertain	0.89	D;.
M_CAP	Benign	0.010	T
MetaRNN	Benign	0.16	T;T
MetaSVM	Benign	-0.99	T
MutationAssessor	Benign	0.55	N;N
PrimateAI	Benign	0.26	T
PROVEAN	Uncertain	-3.7	.;D
REVEL	Benign	0.051
Sift	Benign	0.14	.;T
Sift4G	Benign	0.13	T;T
Polyphen		0.0030	B;B
Vest4		0.17
MutPred		0.31		Loss of methylation at K184 (P = 0.0583);Loss of methylation at K184 (P = 0.0583);
MVP		0.41
MPC		0.10
ClinPred		0.79	D
GERP RS		5.3
Varity_R		0.24
gMVP		0.28

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: rs764264847; hg19: chr2-216809671;