10-75094806-C-G

Variant names:

• chr10-75094806-C-G
• rs3088142
• NM_001363514.2:c.875G>C

Variant summary

Our verdict is Likely benign. The variant received -2 ACMG points: 2P and 4B. PM2 BP4_Strong

The NM_001363514.2(DUSP13B):​c.875G>C​(p.Cys292Ser) 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. 16/22 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. C292Y) has been classified as Benign.

• Frequency: Genomes: not found (cov: 33)
• Consequence: DUSP13B NM_001363514.2 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.236
• Publications: 38 publications found

Genes affected

DUSP13B (HGNC:19681): (dual specificity phosphatase 13B) Members of the protein-tyrosine phosphatase superfamily cooperate with protein kinases to regulate cell proliferation and differentiation. This gene encodes a dual specificity phosphatase that acts on both phosphotyrosine and phosphoserine/threonine residues. The encoded protein is expressed in testis. [provided by RefSeq, Mar 2023]

DUSP13A (HGNC:56772): (dual specificity phosphatase 13A) Members of the protein-tyrosine phosphatase superfamily cooperate with protein kinases to regulate cell proliferation and differentiation. This gene encodes a dual specificity phosphatase that acts on both phosphotyrosine and phosphoserine/threonine residues. The encoded protein is expressed in skeletal muscle. [provided by RefSeq, Mar 2023]

ACMG classification

Our verdict: Likely_benign. The variant received -2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.040029317).

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001363514.2. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	DUSP13B	NM_001363514.2	MANE Select	c.875G>C	p.Cys292Ser	missense	Exon 4 of 4	NP_001350443.1	Q9UII6-5
	DUSP13B	NM_001007273.2		c.746G>C	p.Cys249Ser	missense	Exon 6 of 6	NP_001007274.1	A0A9L9PXN7
	DUSP13B	NM_001320842.2		c.746G>C	p.Cys249Ser	missense	Exon 7 of 7	NP_001307771.1	A0A9L9PXN7

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	DUSP13B	ENST00000478873.7	TSL:5 MANE Select	c.875G>C	p.Cys292Ser	missense	Exon 4 of 4	ENSP00000475626.1	Q9UII6-5
	DUSP13B	ENST00000473072.3	TSL:5	c.1124G>C	p.Cys375Ser	missense	Exon 7 of 7	ENSP00000475732.2	U3KQB7
	DUSP13B	ENST00000472493.6	TSL:1	c.467G>C	p.Cys156Ser	missense	Exon 4 of 4	ENSP00000444580.1	Q9UII6-1

Frequencies

GnomAD3 genomes Cov.: 33

GnomAD4 exome Cov.: 57

GnomAD4 genome Cov.: 33

Alfa AF: 0.00 Hom.: 63632

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.25
BayesDel_addAF	Benign	-0.10	T
BayesDel_noAF	Benign	-0.38
CADD	Benign	7.0
DANN	Benign	0.76
DEOGEN2	Benign	0.19	T
Eigen	Benign	-1.3
Eigen_PC	Benign	-1.2
FATHMM_MKL	Benign	0.32	N
LIST_S2	Benign	0.69	T
M_CAP	Uncertain	0.089	D
MetaRNN	Benign	0.040	T
MetaSVM	Benign	-0.87	T
MutationAssessor	Benign	-0.53	N
PhyloP100		-0.24
PrimateAI	Benign	0.27	T
PROVEAN	Benign	-1.6	N
REVEL	Benign	0.21
Sift	Benign	0.28	T
Sift4G	Benign	0.39	T
Polyphen		0.043	B
Vest4		0.24
MVP		0.048
MPC		0.20
ClinPred		0.11	T
GERP RS		-2.2
Varity_R		0.17
gMVP		0.56
Mutation Taster		=92/8	polymorphism

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: rs3088142; hg19: chr10-76854564;