NM_000138.5(FBN1):c.4159T>G (p.Tyr1387Asp) AND not provided

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: May 20, 2019
Review status:: 1 star out of maximum of 4 stars
criteria provided, single submitter

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV001770386.2

Allele description [Variation Report for NM_000138.5(FBN1):c.4159T>G (p.Tyr1387Asp)]

NM_000138.5(FBN1):c.4159T>G (p.Tyr1387Asp)

Gene:

FBN1:fibrillin 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

15q21.1

Genomic location:

Preferred name:

NM_000138.5(FBN1):c.4159T>G (p.Tyr1387Asp)

HGVS:

NC_000015.10:g.48474306A>C
NG_008805.2:g.176483T>G
NM_000138.5:c.4159T>GMANE SELECT
NP_000129.3:p.Tyr1387Asp
NP_000129.3:p.Tyr1387Asp
LRG_778t1:c.4159T>G
LRG_778:g.176483T>G
LRG_778p1:p.Tyr1387Asp
NC_000015.9:g.48766503A>C
NM_000138.4:c.4159T>G

Protein change:

Y1387D

Links:

dbSNP: rs1555397656

NCBI 1000 Genomes Browser:

rs1555397656

Molecular consequence:

NM_000138.5:c.4159T>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001993525	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Uncertain significance (May 20, 2019)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001993525

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Uncertain significance
(May 20, 2019)

germline

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	yes	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From GeneDx, SCV001993525.2

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

Description

Has not been previously published as pathogenic or benign to our knowledge; In silico analysis, which includes protein predictors and evolutionary conservation, supports a deleterious effect; Not observed in large population cohorts (Lek et al., 2016); Reported in ClinVar as a variant of uncertain significance, but additional evidence is not available (ClinVar Variant ID 439718; Landrum et al., 2016)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Sep 29, 2024

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