NM_015375.3:c.53C>G

Variant names:

• chr1-205211483-G-C
• rs202068245
• NM_015375.3:c.53C>G

Variant summary

Our verdict is Uncertain significance. Variant got 1 ACMG points: 2P and 1B. PM2 BP4

The NM_015375.3(DSTYK):​c.53C>G​(p.Pro18Arg) 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. P18L) has been classified as Likely benign.

• Frequency: Genomes: not found (cov: 33)
• Consequence: DSTYK NM_015375.3 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.983

Genes affected

DSTYK (HGNC:29043): (dual serine/threonine and tyrosine protein kinase) This gene encodes a dual serine/threonine and tyrosine protein kinase which is expressed in multiple tissues. It is thought to function as a regulator of cell death. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]

ACMG classification

Verdict is Uncertain_significance. Variant got 1 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.28101742).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
DSTYK	NM_015375.3	c.53C>G	p.Pro18Arg	missense_variant	Exon 1 of 13	ENST00000367162.8	NP_056190.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
DSTYK	ENST00000367162.8	c.53C>G	p.Pro18Arg	missense_variant	Exon 1 of 13	1	NM_015375.3	ENSP00000356130.3
DSTYK	ENST00000367161.7	c.53C>G	p.Pro18Arg	missense_variant	Exon 1 of 12	1		ENSP00000356129.3

Frequencies

GnomAD3 genomes Cov.: 33

GnomAD4 exome Cov.: 32

GnomAD4 genome Cov.: 33

Bravo AF: 0.00000378

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.13
BayesDel_addAF	Uncertain	0.046	T
BayesDel_noAF	Benign	-0.17
CADD	Benign	19
DANN	Benign	0.92
DEOGEN2	Benign	0.016	.;T
Eigen	Benign	-0.028
Eigen_PC	Benign	0.077
FATHMM_MKL	Benign	0.21	N
LIST_S2	Benign	0.57	T;T
M_CAP	Pathogenic	0.46	D
MetaRNN	Benign	0.28	T;T
MetaSVM	Benign	-0.71	T
MutationAssessor	Benign	1.0	L;L
PrimateAI	Pathogenic	0.86	D
PROVEAN	Benign	-0.18	N;N
REVEL	Benign	0.22
Sift	Benign	0.068	T;T
Sift4G	Benign	0.52	T;T
Polyphen		0.70	P;P
Vest4		0.28
MutPred		0.30		Gain of MoRF binding (P = 0.0034);Gain of MoRF binding (P = 0.0034);
MVP		0.69
MPC		0.38
ClinPred		0.70	D
GERP RS		4.3
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.7
Varity_R		0.045
gMVP		0.31

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: rs202068245; hg19: chr1-205180611;