rs1036477

chr15-48622729-A-G

Variant summary

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

The NM_000138.5(FBN1):c.165-9637T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.24 in 151,908 control chromosomes in the GnomAD database, including 7,137 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 0.24 (7137 hom., cov: 31)
• Consequence: FBN1 NM_000138.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -2.10

Genes affected

FBN1 (HGNC:3603): (fibrillin 1) This gene encodes a member of the fibrillin family of proteins. The encoded preproprotein is proteolytically processed to generate two proteins including the extracellular matrix component fibrillin-1 and the protein hormone asprosin. Fibrillin-1 is an extracellular matrix glycoprotein that serves as a structural component of calcium-binding microfibrils. These microfibrils provide force-bearing structural support in elastic and nonelastic connective tissue throughout the body. Asprosin, secreted by white adipose tissue, has been shown to regulate glucose homeostasis. Mutations in this gene are associated with Marfan syndrome and the related MASS phenotype, as well as ectopia lentis syndrome, Weill-Marchesani syndrome, Shprintzen-Goldberg syndrome and neonatal progeroid syndrome. [provided by RefSeq, Apr 2016]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.92).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.537 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
FBN1	NM_000138.5	c.165-9637T>C		intron_variant		ENST00000316623.10
FBN1	NM_001406716.1	c.165-9637T>C		intron_variant
FBN1	NM_001406717.1	c.165-9637T>C		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
FBN1	ENST00000316623.10	c.165-9637T>C		intron_variant		1	NM_000138.5	P1
FBN1	ENST00000559133.6	c.165-9637T>C		intron_variant, NMD_transcript_variant		1
FBN1	ENST00000537463.6	c.165-9637T>C		intron_variant, NMD_transcript_variant		5
FBN1	ENST00000674301.2	c.165-9637T>C		intron_variant, NMD_transcript_variant

Frequencies

GnomAD3 genomes AF: 0.239 AC: 36333 AN: 151790 Hom.: 7098 Cov.: 31

Gnomad AFR AF: 0.542

Gnomad AMI AF: 0.156

Gnomad AMR AF: 0.179

Gnomad ASJ AF: 0.133

Gnomad EAS AF: 0.273

Gnomad SAS AF: 0.158

Gnomad FIN AF: 0.0713

Gnomad MID AF: 0.182

Gnomad NFE AF: 0.106

Gnomad OTH AF: 0.213

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

GnomAD4 genome AF: 0.240 AC: 36430 AN: 151908 Hom.: 7137 Cov.: 31 AF XY: 0.235 AC XY: 17440 AN XY: 74246

Gnomad4 AFR AF: 0.543

Gnomad4 AMR AF: 0.179

Gnomad4 ASJ AF: 0.133

Gnomad4 EAS AF: 0.274

Gnomad4 SAS AF: 0.156

Gnomad4 FIN AF: 0.0713

Gnomad4 NFE AF: 0.106

Gnomad4 OTH AF: 0.214

Alfa AF: 0.135 Hom.: 2631

Bravo AF: 0.261

Asia WGS AF: 0.265 AC: 919 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.92
Cadd	Benign	0.17
Dann	Benign	0.41

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: rs1036477; hg19: chr15-48914926;