rs7760282

Variant names:

• chr6-166570486-A-C
• rs7760282
• NM_021135.6:c.100-31702T>G

Your query was ambiguous. Multiple possible variants found:

• chr6-166570486-A-C
• chr6-166570486-A-G
• chr6-166570486-A-T

Variant summary

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

The NM_021135.6(RPS6KA2):​c.100-31702T>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.625 in 152,140 control chromosomes in the GnomAD database, including 31,181 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 0.63 (31181 hom., cov: 33)
• Consequence: RPS6KA2 NM_021135.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.28

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=-0.98).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.828 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
RPS6KA2	NM_021135.6	c.100-31702T>G		intron_variant	Intron 1 of 20	ENST00000265678.9	NP_066958.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
RPS6KA2	ENST00000265678.9	c.100-31702T>G		intron_variant	Intron 1 of 20	1	NM_021135.6	ENSP00000265678.4

Frequencies

GnomAD3 genomes AF: 0.625 AC: 95036 AN: 152022 Hom.: 31126 Cov.: 33

Gnomad AFR AF: 0.793

Gnomad AMI AF: 0.477

Gnomad AMR AF: 0.648

Gnomad ASJ AF: 0.580

Gnomad EAS AF: 0.849

Gnomad SAS AF: 0.749

Gnomad FIN AF: 0.483

Gnomad MID AF: 0.649

Gnomad NFE AF: 0.519

Gnomad OTH AF: 0.601

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

GnomAD4 genome AF: 0.625 AC: 95154 AN: 152140 Hom.: 31181 Cov.: 33 AF XY: 0.627 AC XY: 46612 AN XY: 74374

Gnomad4 AFR AF: 0.793

Gnomad4 AMR AF: 0.648

Gnomad4 ASJ AF: 0.580

Gnomad4 EAS AF: 0.848

Gnomad4 SAS AF: 0.748

Gnomad4 FIN AF: 0.483

Gnomad4 NFE AF: 0.519

Gnomad4 OTH AF: 0.604

Alfa AF: 0.498 Hom.: 4255

Bravo AF: 0.646

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.98
CADD	Benign	0.087
DANN	Benign	0.44

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: rs7760282; hg19: chr6-166983974;