NM_003239.5(TGFB3):c.850C>A (p.Pro284Thr) AND See cases

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jan 5, 2022
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:: RCV002287754.1

Allele description [Variation Report for NM_003239.5(TGFB3):c.850C>A (p.Pro284Thr)]

NM_003239.5(TGFB3):c.850C>A (p.Pro284Thr)

Gene:

TGFB3:transforming growth factor beta 3 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

14q24.3

Genomic location:

Preferred name:

NM_003239.5(TGFB3):c.850C>A (p.Pro284Thr)

HGVS:

NC_000014.9:g.75963392G>T
NG_011715.1:g.23358C>A
NM_001329938.2:c.850C>A
NM_001329939.2:c.850C>A
NM_003239.5:c.850C>AMANE SELECT
NP_001316867.1:p.Pro284Thr
NP_001316868.1:p.Pro284Thr
NP_003230.1:p.Pro284Thr
NP_003230.1:p.Pro284Thr
LRG_399t1:c.850C>A
LRG_399:g.23358C>A
LRG_399p1:p.Pro284Thr
NC_000014.8:g.76429735G>T
NM_003239.2:c.850C>A

Protein change:

P284T

Molecular consequence:

NM_001329938.2:c.850C>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001329939.2:c.850C>A - missense variant - [Sequence Ontology: SO:0001583]
NM_003239.5:c.850C>A - missense variant - [Sequence Ontology: SO:0001583]

Observations:

Condition(s)

Name:: See cases [See the Variation display for details]
Identifiers:

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002577949	Institute of Human Genetics, University Hospital Muenster	criteria provided, single submitter (ACMG Guidelines, 2015)	Uncertain significance (Jan 5, 2022)	unknown	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002577949

Institute of Human Genetics, University Hospital Muenster

criteria provided, single submitter

(ACMG Guidelines, 2015)

Uncertain significance
(Jan 5, 2022)

unknown

clinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	unknown	yes	1	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]

PMID:: 25741868
PMCID:: PMC4544753

Details of each submission

From Institute of Human Genetics, University Hospital Muenster, SCV002577949.1

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

Description

ACMG categories: PM2,PP3,BP1

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

Last Updated: Oct 15, 2022

ClinVar

Relating variation to medicine