NM_203446.3(SYNJ1):c.38T>C (p.Leu13Ser) AND not provided

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Mar 5, 2021
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:: RCV001751768.2

Allele description [Variation Report for NM_203446.3(SYNJ1):c.38T>C (p.Leu13Ser)]

NM_203446.3(SYNJ1):c.38T>C (p.Leu13Ser)

Gene:

SYNJ1:synaptojanin 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

21q22.11

Genomic location:

Preferred name:

NM_203446.3(SYNJ1):c.38T>C (p.Leu13Ser)

HGVS:

NC_000021.9:g.32726858A>G
NG_030017.2:g.6182T>C
NM_001160302.2:c.38T>C
NM_001160306.2:c.38T>C
NM_003895.4:c.155T>C
NM_203446.3:c.38T>CMANE SELECT
NP_001153774.1:p.Leu13Ser
NP_001153774.1:p.Leu13Ser
NP_001153778.1:p.Leu13Ser
NP_003886.3:p.Leu52Ser
NP_003886.3:p.Leu52Ser
NP_982271.3:p.Leu13Ser
NC_000021.8:g.34099169A>G
NG_030017.1:g.6183T>C
NM_001160302.1:c.38T>C
NM_003895.3:c.155T>C

Protein change:

L13S

Links:

dbSNP: rs779059079

NCBI 1000 Genomes Browser:

rs779059079

Molecular consequence:

NM_001160302.2:c.38T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001160306.2:c.38T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_003895.4:c.155T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_203446.3:c.38T>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM
Identifiers:: MedGen: C3661900

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001987484	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Uncertain significance (Mar 5, 2021)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001987484

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Uncertain significance
(Mar 5, 2021)

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, SCV001987484.2

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

Description

In silico analysis supports that this missense variant does not alter protein structure/function; This variant is associated with the following publications: (PMID: 28421333)

#	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: May 16, 2025

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