rs534581077

Variant names:

• chr2-76748862-C-G
• rs534581077
• NM_001134745.3:c.1606G>C

Your query was ambiguous. Multiple possible variants found:

• chr2-76748862-C-G
• chr2-76748862-C-T

Variant summary

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

The NM_001134745.3(LRRTM4):​c.1606G>C​(p.Gly536Arg) 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: 32)
• Consequence: LRRTM4 NM_001134745.3 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.79

Genes affected

LRRTM4 (HGNC:19411): (leucine rich repeat transmembrane neuronal 4) Predicted to enable heparan sulfate proteoglycan binding activity. Predicted to be involved in regulation of synapse assembly. Predicted to act upstream of or within AMPA glutamate receptor clustering; positive regulation of synapse assembly; and regulation of presynaptic membrane organization. Predicted to be located in postsynaptic membrane. Predicted to be part of AMPA glutamate receptor complex. Predicted to be active in extracellular matrix; extracellular space; and glutamatergic synapse. Predicted to be integral component of postsynaptic density membrane. [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=0.118879884).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
LRRTM4	NM_001134745.3	c.1606G>C	p.Gly536Arg	missense_variant	Exon 4 of 4	ENST00000409884.6	NP_001128217.1
LRRTM4	NM_001330370.2	c.1609G>C	p.Gly537Arg	missense_variant	Exon 3 of 3		NP_001317299.1
LRRTM4	NM_001282924.3	c.1606G>C	p.Gly536Arg	missense_variant	Exon 4 of 4		NP_001269853.1
LRRTM4	NR_146416.2	n.323G>C		non_coding_transcript_exon_variant	Exon 2 of 2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
LRRTM4	ENST00000409884.6	c.1606G>C	p.Gly536Arg	missense_variant	Exon 4 of 4	1	NM_001134745.3	ENSP00000387297.1
LRRTM4	ENST00000409911.5	c.1609G>C	p.Gly537Arg	missense_variant	Exon 3 of 3	5		ENSP00000387228.1
LRRTM4	ENST00000409093.1	c.1606G>C	p.Gly536Arg	missense_variant	Exon 4 of 4	2		ENSP00000386357.1

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 34

GnomAD4 genome Cov.: 32

Bravo AF: 0.00000378

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.26
BayesDel_addAF	Benign	-0.16	T
BayesDel_noAF	Benign	-0.47
CADD	Benign	21
DANN	Uncertain	0.98
DEOGEN2	Benign	0.0089	T;T;T
Eigen	Benign	-0.090
Eigen_PC	Benign	-0.039
FATHMM_MKL	Uncertain	0.87	D
LIST_S2	Benign	0.73	T;.;T
M_CAP	Benign	0.015	T
MetaRNN	Benign	0.12	T;T;T
MetaSVM	Benign	-1.1	T
MutationAssessor	Benign	0.20	.;N;N
PrimateAI	Uncertain	0.52	T
PROVEAN	Benign	-0.52	N;N;N
REVEL	Benign	0.041
Sift	Benign	0.10	T;T;T
Sift4G	Uncertain	0.050	T;T;T
Polyphen		0.81	.;P;P
Vest4		0.18
MutPred		0.38		.;Gain of solvent accessibility (P = 0.0263);Gain of solvent accessibility (P = 0.0263);
MVP		0.12
MPC		0.80
ClinPred		0.42	T
GERP RS		4.1
Varity_R		0.099
gMVP		0.42

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: rs534581077; hg19: chr2-76975988;