NM_000602.5(SERPINE1):c.217A>G (p.Thr73Ala) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Dec 20, 2023
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:: RCV004453371.1

Allele description [Variation Report for NM_000602.5(SERPINE1):c.217A>G (p.Thr73Ala)]

NM_000602.5(SERPINE1):c.217A>G (p.Thr73Ala)

Gene:

SERPINE1:serpin family E member 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

7q22.1

Genomic location:

Preferred name:

NM_000602.5(SERPINE1):c.217A>G (p.Thr73Ala)

HGVS:

NC_000007.14:g.101128610A>G
NG_013213.1:g.6513A>G
NG_111964.1:g.391A>G
NM_000602.5:c.217A>GMANE SELECT
NM_001386456.1:c.-32-4A>G
NM_001386457.1:c.217A>G
NM_001386458.1:c.217A>G
NM_001386459.1:c.217A>G
NM_001386460.1:c.217A>G
NM_001386461.1:c.217A>G
NM_001386462.1:c.16A>G
NM_001386463.1:c.211A>G
NM_001386464.1:c.217A>G
NM_001386465.1:c.217A>G
NM_001386466.1:c.217A>G
NP_000593.1:p.Thr73Ala
NP_000593.1:p.Thr73Ala
NP_001373386.1:p.Thr73Ala
NP_001373387.1:p.Thr73Ala
NP_001373388.1:p.Thr73Ala
NP_001373389.1:p.Thr73Ala
NP_001373390.1:p.Thr73Ala
NP_001373391.1:p.Thr6Ala
NP_001373392.1:p.Thr71Ala
NP_001373393.1:p.Thr73Ala
NP_001373394.1:p.Thr73Ala
NP_001373395.1:p.Thr73Ala
LRG_597t1:c.217A>G
LRG_597:g.6513A>G
LRG_597p1:p.Thr73Ala
NC_000007.13:g.100771891A>G
NM_000602.3:c.217A>G
NM_000602.4:c.217A>G

Protein change:

T6A

Molecular consequence:

NM_001386456.1:c.-32-4A>G - intron variant - [Sequence Ontology: SO:0001627]
NM_000602.5:c.217A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001386457.1:c.217A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001386458.1:c.217A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001386459.1:c.217A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001386460.1:c.217A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001386461.1:c.217A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001386462.1:c.16A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001386463.1:c.211A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001386464.1:c.217A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001386465.1:c.217A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001386466.1:c.217A>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004947835	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Dec 20, 2023)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004947835

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Dec 20, 2023)

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	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Ambry Genetics, SCV004947835.1

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

Description

The c.217A>G (p.T73A) alteration is located in exon 2 (coding exon 1) of the SERPINE1 gene. This alteration results from a A to G substitution at nucleotide position 217, causing the threonine (T) at amino acid position 73 to be replaced by an alanine (A). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

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

Last Updated: May 7, 2024

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