rs10497337

Positions:

• chr2-168170639-G-A

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_013233.3(STK39):​c.322-3232C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.164 in 152,184 control chromosomes in the GnomAD database, including 2,123 homozygotes. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.16 (2123 hom., cov: 32)
• Consequence: STK39 NM_013233.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.24

Genes affected

STK39 (HGNC:17717): (serine/threonine kinase 39) This gene encodes a serine/threonine kinase that is thought to function in the cellular stress response pathway. The kinase is activated in response to hypotonic stress, leading to phosphorylation of several cation-chloride-coupled cotransporters. The catalytically active kinase specifically activates the p38 MAP kinase pathway, and its interaction with p38 decreases upon cellular stress, suggesting that this kinase may serve as an intermediate in the response to cellular stress. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.81).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.235 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
STK39	NM_013233.3	c.322-3232C>T		intron_variant		ENST00000355999.5	NP_037365.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
STK39	ENST00000355999.5	c.322-3232C>T		intron_variant		1	NM_013233.3	ENSP00000348278.4
STK39	ENST00000697205.1	c.322-3232C>T		intron_variant				ENSP00000513185.1

Frequencies

GnomAD3 genomes AF: 0.164 AC: 25004 AN: 152066 Hom.: 2124 Cov.: 32

Gnomad AFR AF: 0.132

Gnomad AMI AF: 0.111

Gnomad AMR AF: 0.226

Gnomad ASJ AF: 0.145

Gnomad EAS AF: 0.245

Gnomad SAS AF: 0.214

Gnomad FIN AF: 0.158

Gnomad MID AF: 0.191

Gnomad NFE AF: 0.163

Gnomad OTH AF: 0.172

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.164 AC: 25007 AN: 152184 Hom.: 2123 Cov.: 32 AF XY: 0.164 AC XY: 12182 AN XY: 74404

Gnomad4 AFR AF: 0.132

Gnomad4 AMR AF: 0.226

Gnomad4 ASJ AF: 0.145

Gnomad4 EAS AF: 0.246

Gnomad4 SAS AF: 0.213

Gnomad4 FIN AF: 0.158

Gnomad4 NFE AF: 0.163

Gnomad4 OTH AF: 0.174

Alfa AF: 0.164 Hom.: 962

Bravo AF: 0.169

Asia WGS AF: 0.201 AC: 700 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.81
CADD	Benign	6.8
DANN	Benign	0.58

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: rs10497337; hg19: chr2-169027149;