NM_005902.4(SMAD3):c.424C>T (p.Arg142Cys) AND not provided

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Nov 12, 2020
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:: RCV001557706.2

Allele description [Variation Report for NM_005902.4(SMAD3):c.424C>T (p.Arg142Cys)]

NM_005902.4(SMAD3):c.424C>T (p.Arg142Cys)

Gene:

SMAD3:SMAD family member 3 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

15q22.33

Genomic location:

Preferred name:

NM_005902.4(SMAD3):c.424C>T (p.Arg142Cys)

HGVS:

NC_000015.10:g.67165276C>T
NG_011990.1:g.104420C>T
NM_001145102.2:c.109C>T
NM_001145103.2:c.292C>T
NM_005902.4:c.424C>TMANE SELECT
NP_001138574.1:p.Arg37Cys
NP_001138575.1:p.Arg98Cys
NP_005893.1:p.Arg142Cys
NC_000015.9:g.67457614C>T
NC_000015.9:g.67457614C>T
NM_005902.3:c.424C>T

Protein change:

R142C

Links:

dbSNP: rs1253901433

NCBI 1000 Genomes Browser:

rs1253901433

Molecular consequence:

NM_001145102.2:c.109C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001145103.2:c.292C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_005902.4:c.424C>T - 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
SCV001779517	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Uncertain significance (Nov 12, 2020)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001779517

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Uncertain significance
(Nov 12, 2020)

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, SCV001779517.1

#	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; Reported in ClinVar (ClinVar Variant ID# 925560; Landrum et al., 2016); Not observed at a significant frequency in large population cohorts (Lek et al., 2016); In silico analysis supports that this missense variant has a deleterious effect on protein structure/function

#	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

ClinVar

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