NM_005983.4:c.901+98T>G

Variant names:

• chr5-36171831-T-G
• rs7715070
• NM_005983.4:c.901+98T>G

Variant summary

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

The NM_005983.4(SKP2):​c.901+98T>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0922 in 1,220,382 control chromosomes in the GnomAD database, including 15,401 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 0.21 (7773 hom., cov: 32)
  • Exomes 𝑓: 0.075 (7628 hom.)
• Consequence: SKP2 NM_005983.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.296
• Publications: 5 publications found

Genes affected

SKP2 (HGNC:10901): (S-phase kinase associated protein 2) This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbls class; in addition to an F-box, this protein contains 10 tandem leucine-rich repeats. This protein is an essential element of the cyclin A-CDK2 S-phase kinase. It specifically recognizes phosphorylated cyclin-dependent kinase inhibitor 1B (CDKN1B, also referred to as p27 or KIP1) predominantly in S phase and interacts with S-phase kinase-associated protein 1 (SKP1 or p19). In addition, this gene is established as a protooncogene causally involved in the pathogenesis of lymphomas. Alternative splicing of this gene generates three transcript variants encoding different isoforms. [provided by RefSeq, Jul 2011]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.78).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.587 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_005983.4. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SKP2	NM_005983.4	MANE Select	c.901+98T>G		intron	N/A	NP_005974.2
	SKP2	NM_032637.4		c.901+98T>G		intron	N/A	NP_116026.1	Q13309-2
	SKP2	NM_001243120.2		c.259+98T>G		intron	N/A	NP_001230049.1	Q13309-4

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SKP2	ENST00000274255.11	TSL:1 MANE Select	c.901+98T>G		intron	N/A	ENSP00000274255.6	Q13309-1
	SKP2	ENST00000274254.9	TSL:1	c.901+98T>G		intron	N/A	ENSP00000274254.5	Q13309-2
	SKP2	ENST00000855793.1		c.901+98T>G		intron	N/A	ENSP00000525852.1

Frequencies

GnomAD3 genomes AF: 0.210 AC: 31922 AN: 152028 Hom.: 7732 Cov.: 32

Gnomad AFR AF: 0.593

Gnomad AMI AF: 0.0504

Gnomad AMR AF: 0.106

Gnomad ASJ AF: 0.128

Gnomad EAS AF: 0.0535

Gnomad SAS AF: 0.143

Gnomad FIN AF: 0.0325

Gnomad MID AF: 0.139

Gnomad NFE AF: 0.0528

Gnomad OTH AF: 0.170

GnomAD4 exome AF: 0.0753 AC: 80443 AN: 1068234 Hom.: 7628 AF XY: 0.0757 AC XY: 40824 AN XY: 539330

African (AFR) AF: 0.621 AC: 15802 AN: 25446

American (AMR) AF: 0.0681 AC: 2218 AN: 32564

Ashkenazi Jewish (ASJ) AF: 0.117 AC: 2451 AN: 20982

East Asian (EAS) AF: 0.0486 AC: 1701 AN: 34984

South Asian (SAS) AF: 0.140 AC: 9599 AN: 68784

European-Finnish (FIN) AF: 0.0385 AC: 1646 AN: 42792

Middle Eastern (MID) AF: 0.126 AC: 615 AN: 4900

European-Non Finnish (NFE) AF: 0.0525 AC: 41496 AN: 790722

Other (OTH) AF: 0.104 AC: 4915 AN: 47060

GnomAD4 genome AF: 0.210 AC: 32027 AN: 152148 Hom.: 7773 Cov.: 32 AF XY: 0.205 AC XY: 15239 AN XY: 74400

African (AFR) AF: 0.594 AC: 24604 AN: 41444

American (AMR) AF: 0.105 AC: 1611 AN: 15294

Ashkenazi Jewish (ASJ) AF: 0.128 AC: 444 AN: 3472

East Asian (EAS) AF: 0.0534 AC: 277 AN: 5186

South Asian (SAS) AF: 0.144 AC: 694 AN: 4820

European-Finnish (FIN) AF: 0.0325 AC: 345 AN: 10622

Middle Eastern (MID) AF: 0.136 AC: 40 AN: 294

European-Non Finnish (NFE) AF: 0.0528 AC: 3590 AN: 67992

Other (OTH) AF: 0.178 AC: 376 AN: 2112

Alfa AF: 0.154 Hom.: 921

Bravo AF: 0.233

Asia WGS AF: 0.162 AC: 561 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.78
CADD	Benign	4.4
DANN	Benign	0.84
PhyloP100		-0.30
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.1
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: rs7715070; hg19: chr5-36171933;