chr6-166413532-A-G

Position:

• chr6-166413532-A-G

Variant summary

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

The ENST00000265678.9(RPS6KA2):​c.2076+262T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.693 in 152,028 control chromosomes in the GnomAD database, including 36,750 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 0.69 (36750 hom., cov: 31)
• Consequence: RPS6KA2 ENST00000265678.9 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.622

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]

LOC124901460 (HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.94).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.82 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
RPS6KA2	NM_021135.6	c.2076+262T>C		intron_variant		ENST00000265678.9	NP_066958.2
LOC124901460	XR_007059866.1	n.647A>G		non_coding_transcript_exon_variant	1/2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
RPS6KA2	ENST00000265678.9	c.2076+262T>C		intron_variant		1	NM_021135.6	ENSP00000265678	P1

Frequencies

GnomAD3 genomes AF: 0.692 AC: 105171 AN: 151910 Hom.: 36700 Cov.: 31

Gnomad AFR AF: 0.711

Gnomad AMI AF: 0.577

Gnomad AMR AF: 0.730

Gnomad ASJ AF: 0.755

Gnomad EAS AF: 0.813

Gnomad SAS AF: 0.842

Gnomad FIN AF: 0.573

Gnomad MID AF: 0.785

Gnomad NFE AF: 0.668

Gnomad OTH AF: 0.724

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

GnomAD4 genome AF: 0.693 AC: 105281 AN: 152028 Hom.: 36750 Cov.: 31 AF XY: 0.691 AC XY: 51363 AN XY: 74304

Gnomad4 AFR AF: 0.711

Gnomad4 AMR AF: 0.730

Gnomad4 ASJ AF: 0.755

Gnomad4 EAS AF: 0.814

Gnomad4 SAS AF: 0.842

Gnomad4 FIN AF: 0.573

Gnomad4 NFE AF: 0.668

Gnomad4 OTH AF: 0.728

Alfa AF: 0.680 Hom.: 5930

Bravo AF: 0.703

Asia WGS AF: 0.810 AC: 2816 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.94
CADD	Benign	0.015
DANN	Benign	0.64

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: rs2235296; hg19: chr6-166827020;