U.S. flag

An official website of the United States government

NM_005343.4(HRAS):c.41T>G (p.Val14Gly) AND Costello syndrome

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jun 17, 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:
RCV000810329.8

Allele description [Variation Report for NM_005343.4(HRAS):c.41T>G (p.Val14Gly)]

NM_005343.4(HRAS):c.41T>G (p.Val14Gly)

Genes:
HRAS:HRas proto-oncogene, GTPase [Gene - OMIM - HGNC]
LRRC56:leucine rich repeat containing 56 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
11p15.5
Genomic location:
Preferred name:
NM_005343.4(HRAS):c.41T>G (p.Val14Gly)
HGVS:
  • NC_000011.10:g.534282A>C
  • NG_007666.1:g.6269T>G
  • NM_001130442.3:c.41T>G
  • NM_001318054.2:c.-279T>G
  • NM_005343.4:c.41T>GMANE SELECT
  • NM_176795.5:c.41T>G
  • NP_001123914.1:p.Val14Gly
  • NP_005334.1:p.Val14Gly
  • NP_789765.1:p.Val14Gly
  • LRG_506t1:c.41T>G
  • LRG_506:g.6269T>G
  • LRG_506p1:p.Val14Gly
  • NC_000011.9:g.534282A>C
  • NM_005343.2:c.41T>G
Protein change:
V14G
Links:
dbSNP: rs1589793707
NCBI 1000 Genomes Browser:
rs1589793707
Molecular consequence:
  • NM_001318054.2:c.-279T>G - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001130442.3:c.41T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_005343.4:c.41T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_176795.5:c.41T>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Costello syndrome (CSTLO)
Synonyms:
FACIOCUTANEOSKELETAL SYNDROME; FCS SYNDROME
Identifiers:
MONDO: MONDO:0009026; MedGen: C0587248; Orphanet: 3071; OMIM: 218040

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000950524Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(Jun 17, 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

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group, Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9..

PubMed [citation]
PMID:
28492532
PMCID:
PMC5632818

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV000950524.5

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)

Description

This sequence change replaces valine with glycine at codon 14 of the HRAS protein (p.Val14Gly). The valine residue is highly conserved and there is a moderate physicochemical difference between valine and glycine. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals with HRAS-related disease. Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be disruptive, but these predictions have not been confirmed by published functional studies and their clinical significance is uncertain. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Feb 25, 2025