rs1807984

Positions:

• chr2-168222380-T-G

Variant summary

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

The NM_013233.3(STK39):​c.208+24848A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.385 in 152,116 control chromosomes in the GnomAD database, including 12,246 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 0.38 (12246 hom., cov: 33)
• Consequence: STK39 NM_013233.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.238

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=-0.82).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.479 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
STK39	NM_013233.3	c.208+24848A>C		intron_variant		ENST00000355999.5

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
STK39	ENST00000355999.5	c.208+24848A>C		intron_variant		1	NM_013233.3	P1
STK39	ENST00000697205.1	c.208+24848A>C		intron_variant

Frequencies

GnomAD3 genomes AF: 0.385 AC: 58485 AN: 151998 Hom.: 12243 Cov.: 33

Gnomad AFR AF: 0.264

Gnomad AMI AF: 0.476

Gnomad AMR AF: 0.308

Gnomad ASJ AF: 0.458

Gnomad EAS AF: 0.131

Gnomad SAS AF: 0.357

Gnomad FIN AF: 0.436

Gnomad MID AF: 0.386

Gnomad NFE AF: 0.483

Gnomad OTH AF: 0.402

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

GnomAD4 genome AF: 0.385 AC: 58505 AN: 152116 Hom.: 12246 Cov.: 33 AF XY: 0.380 AC XY: 28285 AN XY: 74382

Gnomad4 AFR AF: 0.264

Gnomad4 AMR AF: 0.308

Gnomad4 ASJ AF: 0.458

Gnomad4 EAS AF: 0.130

Gnomad4 SAS AF: 0.359

Gnomad4 FIN AF: 0.436

Gnomad4 NFE AF: 0.483

Gnomad4 OTH AF: 0.398

Alfa AF: 0.426 Hom.: 1795

Bravo AF: 0.367

Asia WGS AF: 0.256 AC: 890 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.82
CADD	Benign	6.2
DANN	Benign	0.50

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: rs1807984; hg19: chr2-169078890;