NM_001382779.1:c.1301+5667A>G

Variant names:

• chr16-30936251-A-G
• rs7200879
• NM_001382779.1:c.1301+5667A>G

Variant summary

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

The NM_001382779.1(FBXL19):​c.1301+5667A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.224 in 152,060 control chromosomes in the GnomAD database, including 4,550 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 0.22 (4550 hom., cov: 31)
• Consequence: FBXL19 NM_001382779.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.722
• Publications: 23 publications found

Genes affected

FBXL19 (HGNC:25300): (F-box and leucine rich repeat protein 19) This gene encodes a member of the Skp1-Cullin-F-box family of E3 ubiquitin ligases. The encoded protein is reported to bind to the transmembrane receptor interleukin 1 receptor-like 1 and regulate its ubiquitination and degradation. This protein has been linked to the regulation of pulmonary inflammation and psoriasis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.95).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.628 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001382779.1. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	FBXL19	NM_001382779.1	MANE Select	c.1301+5667A>G		intron	N/A	NP_001369708.1
	FBXL19	NM_001099784.3		c.1361+5667A>G		intron	N/A	NP_001093254.2
	FBXL19	NM_001382780.1		c.1238+5667A>G		intron	N/A	NP_001369709.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	FBXL19	ENST00000338343.10	TSL:5 MANE Select	c.1301+5667A>G		intron	N/A	ENSP00000339712.4
	FBXL19	ENST00000427128.5	TSL:1	c.1034+5667A>G		intron	N/A	ENSP00000397913.1
	FBXL19	ENST00000562319.7	TSL:2	c.1361+5667A>G		intron	N/A	ENSP00000455529.2

Frequencies

GnomAD3 genomes AF: 0.224 AC: 34015 AN: 151942 Hom.: 4551 Cov.: 31

Gnomad AFR AF: 0.124

Gnomad AMI AF: 0.297

Gnomad AMR AF: 0.303

Gnomad ASJ AF: 0.188

Gnomad EAS AF: 0.0874

Gnomad SAS AF: 0.649

Gnomad FIN AF: 0.255

Gnomad MID AF: 0.123

Gnomad NFE AF: 0.244

Gnomad OTH AF: 0.223

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

GnomAD4 genome AF: 0.224 AC: 34031 AN: 152060 Hom.: 4550 Cov.: 31 AF XY: 0.233 AC XY: 17289 AN XY: 74336

African (AFR) AF: 0.123 AC: 5125 AN: 41500

American (AMR) AF: 0.304 AC: 4632 AN: 15244

Ashkenazi Jewish (ASJ) AF: 0.188 AC: 651 AN: 3470

East Asian (EAS) AF: 0.0871 AC: 451 AN: 5180

South Asian (SAS) AF: 0.647 AC: 3120 AN: 4820

European-Finnish (FIN) AF: 0.255 AC: 2696 AN: 10576

Middle Eastern (MID) AF: 0.122 AC: 36 AN: 294

European-Non Finnish (NFE) AF: 0.244 AC: 16569 AN: 67956

Other (OTH) AF: 0.228 AC: 481 AN: 2112

Alfa AF: 0.236 Hom.: 9189

Bravo AF: 0.212

Asia WGS AF: 0.387 AC: 1341 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.95
CADD	Benign	0.21
DANN	Benign	0.31
PhyloP100		-0.72
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: rs7200879; hg19: chr16-30947572;