NM_021135.6:c.907+8982T>G

Variant names:

• chr6-166479851-A-C
• rs4709117
• NM_021135.6:c.907+8982T>G

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_021135.6(RPS6KA2):​c.907+8982T>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.3 in 151,806 control chromosomes in the GnomAD database, including 7,057 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 0.30 (7057 hom., cov: 32)
• Consequence: RPS6KA2 NM_021135.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.661
• Publications: 5 publications found

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

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.03).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.528 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
RPS6KA2	NM_021135.6	c.907+8982T>G		intron_variant	Intron 10 of 20	ENST00000265678.9	NP_066958.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
RPS6KA2	ENST00000265678.9	c.907+8982T>G		intron_variant	Intron 10 of 20	1	NM_021135.6	ENSP00000265678.4

Frequencies

GnomAD3 genomes AF: 0.300 AC: 45455 AN: 151686 Hom.: 7042 Cov.: 32

Gnomad AFR AF: 0.315

Gnomad AMI AF: 0.387

Gnomad AMR AF: 0.273

Gnomad ASJ AF: 0.312

Gnomad EAS AF: 0.545

Gnomad SAS AF: 0.396

Gnomad FIN AF: 0.292

Gnomad MID AF: 0.325

Gnomad NFE AF: 0.270

Gnomad OTH AF: 0.303

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

GnomAD4 genome AF: 0.300 AC: 45501 AN: 151806 Hom.: 7057 Cov.: 32 AF XY: 0.302 AC XY: 22403 AN XY: 74190

African (AFR) AF: 0.315 AC: 13035 AN: 41384

American (AMR) AF: 0.274 AC: 4182 AN: 15264

Ashkenazi Jewish (ASJ) AF: 0.312 AC: 1079 AN: 3460

East Asian (EAS) AF: 0.545 AC: 2785 AN: 5108

South Asian (SAS) AF: 0.397 AC: 1912 AN: 4822

European-Finnish (FIN) AF: 0.292 AC: 3068 AN: 10520

Middle Eastern (MID) AF: 0.320 AC: 94 AN: 294

European-Non Finnish (NFE) AF: 0.270 AC: 18344 AN: 67936

Other (OTH) AF: 0.308 AC: 649 AN: 2106

Alfa AF: 0.279 Hom.: 23130

Bravo AF: 0.303

Asia WGS AF: 0.421 AC: 1468 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	2.2
DANN	Benign	0.71
PhyloP100		-0.66
Mutation Taster		=100/0	polymorphism (auto)

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: rs4709117; hg19: chr6-166893339;