1-1632333-C-G

Variant names:

• chr1-1632333-C-G
• NM_006983.2:c.115C>G

Variant summary

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

The NM_006983.2(MMP23B):​c.115C>G​(p.Arg39Gly) 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. 14/20 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Uncertain significance (★).

• Frequency: Genomes: not found (cov: 29)
• Consequence: MMP23B NM_006983.2 missense
• Clinical Significance: Uncertain significance criteria provided, single submitter U:1
• Conservation: PhyloP100: -0.944

Genes affected

MMP23B (HGNC:7171): (matrix metallopeptidase 23B) This gene (MMP23B) encodes a member of the matrix metalloproteinase (MMP) family, and it is part of a duplicated region of chromosome 1p36.3. Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. This gene belongs to the more telomeric copy of the duplicated region. [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=0.15594521).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
MMP23B	NM_006983.2	c.115C>G	p.Arg39Gly	missense_variant	Exon 1 of 8	ENST00000356026.10	NP_008914.1
MMP23B	XM_047432837.1	c.115C>G	p.Arg39Gly	missense_variant	Exon 1 of 8		XP_047288793.1
MMP23B	XM_047432838.1	c.115C>G	p.Arg39Gly	missense_variant	Exon 1 of 8		XP_047288794.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
MMP23B	ENST00000356026.10	c.115C>G	p.Arg39Gly	missense_variant	Exon 1 of 8	1	NM_006983.2	ENSP00000348308.5
MMP23B	ENST00000378675.7	c.115C>G	p.Arg39Gly	missense_variant	Exon 1 of 7	1		ENSP00000367945.3
MMP23B	ENST00000472264.1	c.115C>G	p.Arg39Gly	missense_variant	Exon 1 of 3	3		ENSP00000424976.1
MMP23B	ENST00000512731.5	n.115C>G		non_coding_transcript_exon_variant	Exon 1 of 6	2		ENSP00000423780.1

Frequencies

GnomAD3 genomes Cov.: 29

GnomAD4 exome Cov.: 32

GnomAD4 genome Cov.: 29

ClinVar

Significance: Uncertain significance

Submissions summary: Uncertain:1

Revision: criteria provided, single submitter

Submissions by phenotype

not specified Uncertain:1

Dec 22, 2023

Ambry Genetics

Significance: Uncertain significance

Review Status: criteria provided, single submitter

Collection Method: clinical testing

The c.115C>G (p.R39G) alteration is located in exon 1 (coding exon 1) of the MMP23B gene. This alteration results from a C to G substitution at nucleotide position 115, causing the arginine (R) at amino acid position 39 to be replaced by a glycine (G). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear. -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.057
BayesDel_addAF	Benign	-0.19	T
BayesDel_noAF	Benign	-0.52
CADD	Benign	12
DANN	Benign	0.80
DEOGEN2	Benign	0.091	T;.;.
Eigen	Benign	-1.0
Eigen_PC	Benign	-1.1
FATHMM_MKL	Benign	0.040	N
LIST_S2	Benign	0.58	T;T;T
M_CAP	Benign	0.045	D
MetaRNN	Benign	0.16	T;T;T
MetaSVM	Benign	-1.1	T
MutationAssessor	Benign	0.55	N;.;.
PrimateAI	Uncertain	0.69	T
PROVEAN	Benign	0.18	N;D;N
REVEL	Benign	0.081
Sift	Benign	0.065	T;T;D
Sift4G	Benign	0.47	T;T;T
Polyphen		0.020	B;.;B
Vest4		0.13
MutPred		0.53		Loss of stability (P = 0.0313);Loss of stability (P = 0.0313);Loss of stability (P = 0.0313);
MVP		0.17
ClinPred		0.067	T
GERP RS		-2.3
Varity_R		0.065
gMVP		0.39

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

No publications associated with this variant yet.

Other links and lift over

hg19: chr1-1567712;