NM_005633.4(SOS1):c.1286T>C (p.Ile429Thr) AND Noonan syndrome and Noonan-related syndrome

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Apr 1, 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:: RCV001813710.3

Allele description [Variation Report for NM_005633.4(SOS1):c.1286T>C (p.Ile429Thr)]

NM_005633.4(SOS1):c.1286T>C (p.Ile429Thr)

Gene:

SOS1:SOS Ras/Rac guanine nucleotide exchange factor 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

2p22.1

Genomic location:

Preferred name:

NM_005633.4(SOS1):c.1286T>C (p.Ile429Thr)

HGVS:

NC_000002.12:g.39023142A>G
NG_007530.1:g.102322T>C
NM_001382394.1:c.1265T>C
NM_001382395.1:c.1286T>C
NM_005633.4:c.1286T>CMANE SELECT
NP_001369323.1:p.Ile422Thr
NP_001369324.1:p.Ile429Thr
NP_005624.2:p.Ile429Thr
LRG_754t1:c.1286T>C
LRG_754:g.102322T>C
NC_000002.11:g.39250283A>G
NM_005633.3:c.1286T>C

Protein change:

I422T

Links:

dbSNP: rs755862687

NCBI 1000 Genomes Browser:

rs755862687

Molecular consequence:

NM_001382394.1:c.1265T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001382395.1:c.1286T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_005633.4:c.1286T>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Noonan syndrome and Noonan-related syndrome
Identifiers:: MONDO: MONDO:0020297; MedGen: C5681679; Orphanet: 98733

Recent activity

Clear Turn Off Turn On

OMIM Links for GEO Profiles (Select 131381672) (2)
OMIM

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Help

Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002060900	Genome Diagnostics Laboratory, The Hospital for Sick Children	criteria provided, single submitter (ACMG Guidelines, 2015)	Uncertain significance (Apr 1, 2019)	germline	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

SCV002060900

Genome Diagnostics Laboratory, The Hospital for Sick Children

criteria provided, single submitter

(ACMG Guidelines, 2015)

Uncertain significance
(Apr 1, 2019)

germline

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	germline	unknown	not provided	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 Genome Diagnostics Laboratory, The Hospital for Sick Children, SCV002060900.1

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

#	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: Dec 24, 2023

ClinVar

Relating variation to medicine