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NM_007373.4(SHOC2):c.457C>T (p.Leu153=) AND Noonan syndrome and Noonan-related syndrome

Germline classification:
Benign (1 submission)
Last evaluated:
Mar 30, 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:
RCV001813389.4

Allele description [Variation Report for NM_007373.4(SHOC2):c.457C>T (p.Leu153=)]

NM_007373.4(SHOC2):c.457C>T (p.Leu153=)

Gene:
SHOC2:SHOC2 leucine rich repeat scaffold protein [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
10q25.2
Genomic location:
Preferred name:
NM_007373.4(SHOC2):c.457C>T (p.Leu153=)
Other names:
p.L153L:CTA>TTA; NM_007373.3(SHOC2):c.457C>T
HGVS:
  • NC_000010.11:g.110964815C>T
  • NG_028922.1:g.50273C>T
  • NM_001269039.3:c.457C>T
  • NM_001324336.2:c.457C>T
  • NM_001324337.2:c.457C>T
  • NM_007373.4:c.457C>TMANE SELECT
  • NP_001255968.1:p.Leu153=
  • NP_001311265.1:p.Leu153=
  • NP_001311266.1:p.Leu153=
  • NP_031399.2:p.Leu153=
  • NP_031399.2:p.Leu153=
  • LRG_753t1:c.457C>T
  • LRG_753:g.50273C>T
  • LRG_753p1:p.Leu153=
  • NC_000010.10:g.112724573C>T
  • NM_007373.3:c.457C>T
  • p.Leu153Leu
Links:
dbSNP: rs34081996
NCBI 1000 Genomes Browser:
rs34081996
Molecular consequence:
  • NM_001269039.3:c.457C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001324336.2:c.457C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001324337.2:c.457C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_007373.4:c.457C>T - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

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

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002060626Genome Diagnostics Laboratory, The Hospital for Sick Children
criteria provided, single submitter

(ACMG Guidelines, 2015)		Benign
(Mar 30, 2021) 		germlineclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical 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, SCV002060626.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Oct 20, 2024