NM_002406.4:c.1141C>A

Variant names:

• chr5-180791831-G-T
• NM_002406.4:c.1141C>A

Variant summary

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

The NM_002406.4(MGAT1):​c.1141C>A​(p.Leu381Met) 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. 14/21 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: not found (cov: 33)
• Consequence: MGAT1 NM_002406.4 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.39

Genes affected

MGAT1 (HGNC:7044): (alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase) There are believed to be over 100 different glycosyltransferases involved in the synthesis of protein-bound and lipid-bound oligosaccharides. UDP-N-acetylglucosamine:alpha-3-D-mannoside beta-1,2-N-acetylglucosaminyltransferase I is a medial-Golgi enzyme essential for the synthesis of hybrid and complex N-glycans. The protein, encoded by a single exon, shows typical features of a type II transmembrane protein. The protein is believed to be essential for normal embryogenesis. Several variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]

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=0.17054275).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
MGAT1	NM_002406.4	c.1141C>A	p.Leu381Met	missense_variant	Exon 2 of 2	ENST00000307826.5	NP_002397.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
MGAT1	ENST00000307826.5	c.1141C>A	p.Leu381Met	missense_variant	Exon 2 of 2	1	NM_002406.4	ENSP00000311888.4

Frequencies

GnomAD3 genomes Cov.: 33

GnomAD4 exome Cov.: 36

GnomAD4 genome Cov.: 33

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.12
BayesDel_addAF	Benign	-0.050	T
BayesDel_noAF	Benign	-0.31
CADD	Benign	22
DANN	Uncertain	0.98
DEOGEN2	Benign	0.33	T;T;T;T;T
Eigen	Benign	-0.14
Eigen_PC	Benign	0.0023
FATHMM_MKL	Uncertain	0.88	D
LIST_S2	Benign	0.54	.;.;.;T;.
M_CAP	Benign	0.026	D
MetaRNN	Benign	0.17	T;T;T;T;T
MetaSVM	Benign	-0.37	T
MutationAssessor	Benign	1.8	L;L;L;L;L
PrimateAI	Uncertain	0.50	T
PROVEAN	Benign	0.47	N;N;N;N;N
REVEL	Benign	0.19
Sift	Benign	0.16	T;T;T;T;T
Sift4G	Benign	0.17	T;T;T;T;T
Polyphen		0.063	B;B;B;B;B
Vest4		0.22
MutPred		0.34		Gain of methylation at K379 (P = 0.0585);Gain of methylation at K379 (P = 0.0585);Gain of methylation at K379 (P = 0.0585);Gain of methylation at K379 (P = 0.0585);Gain of methylation at K379 (P = 0.0585);
MVP		0.60
MPC		0.86
ClinPred		0.17	T
GERP RS		4.0
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.1
Varity_R		0.061
gMVP		0.25

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.030		Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

No publications associated with this variant yet.

Other links and lift over

hg19: chr5-180218831;