rs723397

chr5-108012342-C-T

Variant summary

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

The NM_001163315.3(FBXL17):c.1822+8583G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.144 in 152,104 control chromosomes in the GnomAD database, including 1,646 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 0.14 (1646 hom., cov: 32)
• Consequence: FBXL17 NM_001163315.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.633

Genes affected

FBXL17 (HGNC:13615): (F-box and leucine rich repeat protein 17) Members of the F-box protein family, such as FBXL17, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box proteins interact with SKP1 through the F box, and they interact with ubiquitination targets through other protein interaction domains (Jin et al., 2004 [PubMed 15520277]).[supplied by OMIM, Mar 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.168 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
FBXL17	NM_001163315.3	c.1822+8583G>A		intron_variant		ENST00000542267.7
FBXL17	XM_005272048.5	c.1822+8583G>A		intron_variant
FBXL17	XM_011543574.4	c.1822+8583G>A		intron_variant
FBXL17	XM_011543575.3	c.1822+8583G>A		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
FBXL17	ENST00000542267.7	c.1822+8583G>A		intron_variant		1	NM_001163315.3	P1
FBXL17	ENST00000496714.2	c.830+8583G>A		intron_variant		1

Frequencies

GnomAD3 genomes AF: 0.144 AC: 21942 AN: 151986 Hom.: 1644 Cov.: 32

Gnomad AFR AF: 0.131

Gnomad AMI AF: 0.320

Gnomad AMR AF: 0.160

Gnomad ASJ AF: 0.0697

Gnomad EAS AF: 0.178

Gnomad SAS AF: 0.0698

Gnomad FIN AF: 0.179

Gnomad MID AF: 0.0892

Gnomad NFE AF: 0.149

Gnomad OTH AF: 0.132

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

GnomAD4 genome AF: 0.144 AC: 21961 AN: 152104 Hom.: 1646 Cov.: 32 AF XY: 0.146 AC XY: 10838 AN XY: 74360

Gnomad4 AFR AF: 0.131

Gnomad4 AMR AF: 0.160

Gnomad4 ASJ AF: 0.0697

Gnomad4 EAS AF: 0.177

Gnomad4 SAS AF: 0.0697

Gnomad4 FIN AF: 0.179

Gnomad4 NFE AF: 0.149

Gnomad4 OTH AF: 0.131

Alfa AF: 0.142 Hom.: 902

Bravo AF: 0.146

Asia WGS AF: 0.138 AC: 480 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
Cadd	Benign	0.71
Dann	Benign	0.27

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: rs723397; hg19: chr5-107348043;