rs3799631

chr6-166546666-T-Cchr6-166546666-T-G

Variant summary

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

The NM_021135.6(RPS6KA2):c.100-7882A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.412 in 151,922 control chromosomes in the GnomAD database, including 13,579 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 0.41 (13579 hom., cov: 31)
• Consequence: RPS6KA2 NM_021135.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.350

Genes affected

RPS6KA2 (HGNC:10431): (ribosomal protein S6 kinase A2) This gene encodes a member of the RSK (ribosomal S6 kinase) family of serine/threonine kinases. This kinase contains two non-identical kinase catalytic domains and phosphorylates various substrates, including members of the mitogen-activated kinase (MAPK) signalling pathway. The activity of this protein has been implicated in controlling cell growth and differentiation. Alternative splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jan 2016]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.609 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
RPS6KA2	NM_021135.6	c.100-7882A>G		intron_variant		ENST00000265678.9

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
RPS6KA2	ENST00000265678.9	c.100-7882A>G		intron_variant		1	NM_021135.6	P1

Frequencies

GnomAD3 genomes AF: 0.412 AC: 62529 AN: 151804 Hom.: 13581 Cov.: 31

Gnomad AFR AF: 0.538

Gnomad AMI AF: 0.363

Gnomad AMR AF: 0.403

Gnomad ASJ AF: 0.390

Gnomad EAS AF: 0.627

Gnomad SAS AF: 0.284

Gnomad FIN AF: 0.306

Gnomad MID AF: 0.392

Gnomad NFE AF: 0.348

Gnomad OTH AF: 0.402

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

GnomAD4 genome AF: 0.412 AC: 62549 AN: 151922 Hom.: 13579 Cov.: 31 AF XY: 0.410 AC XY: 30440 AN XY: 74264

Gnomad4 AFR AF: 0.538

Gnomad4 AMR AF: 0.403

Gnomad4 ASJ AF: 0.390

Gnomad4 EAS AF: 0.627

Gnomad4 SAS AF: 0.281

Gnomad4 FIN AF: 0.306

Gnomad4 NFE AF: 0.348

Gnomad4 OTH AF: 0.404

Alfa AF: 0.355 Hom.: 5399

Bravo AF: 0.430

Asia WGS AF: 0.443 AC: 1541 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
Cadd	Benign	0.64
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: rs3799631; hg19: chr6-166960154;