NM_001999.4:c.7771A>C

Variant names:

• chr5-128273909-T-G
• rs869025429
• NM_001999.4:c.7771A>C

Variant summary

Our verdict is Uncertain significance. Variant got 1 ACMG points: 3P and 2B. PM2 PP3 BP6_Moderate

The NM_001999.4(FBN2):​c.7771A>C​(p.Thr2591Pro) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a pathogenic outcome for this variant. Variant has been reported in ClinVar as Likely benign (★).

• Frequency: Genomes: not found (cov: 32)
• Consequence: FBN2 NM_001999.4 missense
• Clinical Significance: Likely benign criteria provided, single submitter B:1
• Conservation: PhyloP100: 2.89

Genes affected

FBN2 (HGNC:3604): (fibrillin 2) The protein encoded by this gene is a component of connective tissue microfibrils and may be involved in elastic fiber assembly. Mutations in this gene cause congenital contractural arachnodactyly. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Uncertain_significance. Variant got 1 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• PP3: MetaRNN computational evidence supports a deleterious effect, 0.793
• BP6: Variant 5-128273909-T-G is Benign according to our data. Variant chr5-128273909-T-G is described in ClinVar as [Likely_benign]. Clinvar id is 547363.Status of the report is criteria_provided_single_submitter, 1 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
FBN2	NM_001999.4	c.7771A>C	p.Thr2591Pro	missense_variant	Exon 61 of 65	ENST00000262464.9	NP_001990.2
FBN2	XM_017009228.3	c.7618A>C	p.Thr2540Pro	missense_variant	Exon 60 of 64		XP_016864717.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
FBN2	ENST00000262464.9	c.7771A>C	p.Thr2591Pro	missense_variant	Exon 61 of 65	1	NM_001999.4	ENSP00000262464.4
FBN2	ENST00000703783.1	n.4555A>C		non_coding_transcript_exon_variant	Exon 36 of 38
FBN2	ENST00000703784.1	n.-63A>C		upstream_gene_variant

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 31

GnomAD4 genome Cov.: 32

ClinVar

Significance: Likely benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

Submissions by phenotype

Connective tissue disorder Benign:1

Nov 01, 2016

Center for Human Genetics, Inc, Center for Human Genetics, Inc

Significance: Likely benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

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Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Pathogenic	0.66
BayesDel_addAF	Pathogenic	0.28	D
BayesDel_noAF	Pathogenic	0.16
CADD	Uncertain	26
DANN	Uncertain	1.0
DEOGEN2	Pathogenic	0.89	D;.;D
Eigen	Uncertain	0.67
Eigen_PC	Uncertain	0.59
FATHMM_MKL	Uncertain	0.94	D
LIST_S2	Uncertain	0.94	D;.;.
M_CAP	Pathogenic	0.32	D
MetaRNN	Pathogenic	0.79	D;D;D
MetaSVM	Pathogenic	1.1	D
MutationAssessor	Pathogenic	3.6	H;.;H
PrimateAI	Uncertain	0.63	T
PROVEAN	Uncertain	-4.3	D;.;D
REVEL	Pathogenic	0.83
Sift	Uncertain	0.010	D;.;D
Polyphen		0.86	P;.;P
Vest4		0.54
MutPred		0.71		Gain of catalytic residue at T2591 (P = 0.0829);.;Gain of catalytic residue at T2591 (P = 0.0829);
MVP		0.84
MPC		0.76
ClinPred		0.99	D
GERP RS		4.9
Varity_R		0.89
gMVP		0.72

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: rs869025429; hg19: chr5-127609601;