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NM_020975.6(RET):c.2286G>C (p.Glu762Asp) AND Hereditary cancer-predisposing syndrome

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jul 27, 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:
RCV001015065.3

Allele description [Variation Report for NM_020975.6(RET):c.2286G>C (p.Glu762Asp)]

NM_020975.6(RET):c.2286G>C (p.Glu762Asp)

Gene:
RET:ret proto-oncogene [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
10q11.21
Genomic location:
Preferred name:
NM_020975.6(RET):c.2286G>C (p.Glu762Asp)
HGVS:
  • NC_000010.11:g.43118374G>C
  • NG_007489.1:g.46306G>C
  • NM_000323.2:c.2286G>C
  • NM_001355216.2:c.1524G>C
  • NM_001406743.1:c.2286G>C
  • NM_001406744.1:c.2286G>C
  • NM_001406759.1:c.2286G>C
  • NM_001406760.1:c.2286G>C
  • NM_001406761.1:c.2157G>C
  • NM_001406762.1:c.2157G>C
  • NM_001406763.1:c.2151G>C
  • NM_001406764.1:c.2157G>C
  • NM_001406765.1:c.2151G>C
  • NM_001406766.1:c.1998G>C
  • NM_001406767.1:c.1998G>C
  • NM_001406768.1:c.2022G>C
  • NM_001406769.1:c.1890G>C
  • NM_001406770.1:c.1998G>C
  • NM_001406771.1:c.1848G>C
  • NM_001406772.1:c.1890G>C
  • NM_001406773.1:c.1848G>C
  • NM_001406774.1:c.1761G>C
  • NM_001406775.1:c.1560G>C
  • NM_001406776.1:c.1560G>C
  • NM_001406777.1:c.1560G>C
  • NM_001406778.1:c.1560G>C
  • NM_001406779.1:c.1389G>C
  • NM_001406780.1:c.1389G>C
  • NM_001406781.1:c.1389G>C
  • NM_001406782.1:c.1389G>C
  • NM_001406783.1:c.1260G>C
  • NM_001406784.1:c.1296G>C
  • NM_001406785.1:c.1269G>C
  • NM_001406786.1:c.1260G>C
  • NM_001406787.1:c.1254G>C
  • NM_001406788.1:c.1101G>C
  • NM_001406789.1:c.1101G>C
  • NM_001406790.1:c.1101G>C
  • NM_001406791.1:c.981G>C
  • NM_001406792.1:c.837G>C
  • NM_001406793.1:c.837G>C
  • NM_001406794.1:c.837G>C
  • NM_020629.2:c.2286G>C
  • NM_020630.7:c.2286G>C
  • NM_020975.6:c.2286G>CMANE SELECT
  • NP_000314.1:p.Glu762Asp
  • NP_001342145.1:p.Glu508Asp
  • NP_001342145.1:p.Glu508Asp
  • NP_001393672.1:p.Glu762Asp
  • NP_001393673.1:p.Glu762Asp
  • NP_001393688.1:p.Glu762Asp
  • NP_001393689.1:p.Glu762Asp
  • NP_001393690.1:p.Glu719Asp
  • NP_001393691.1:p.Glu719Asp
  • NP_001393692.1:p.Glu717Asp
  • NP_001393693.1:p.Glu719Asp
  • NP_001393694.1:p.Glu717Asp
  • NP_001393695.1:p.Glu666Asp
  • NP_001393696.1:p.Glu666Asp
  • NP_001393697.1:p.Glu674Asp
  • NP_001393698.1:p.Glu630Asp
  • NP_001393699.1:p.Glu666Asp
  • NP_001393700.1:p.Glu616Asp
  • NP_001393701.1:p.Glu630Asp
  • NP_001393702.1:p.Glu616Asp
  • NP_001393703.1:p.Glu587Asp
  • NP_001393704.1:p.Glu520Asp
  • NP_001393705.1:p.Glu520Asp
  • NP_001393706.1:p.Glu520Asp
  • NP_001393707.1:p.Glu520Asp
  • NP_001393708.1:p.Glu463Asp
  • NP_001393709.1:p.Glu463Asp
  • NP_001393710.1:p.Glu463Asp
  • NP_001393711.1:p.Glu463Asp
  • NP_001393712.1:p.Glu420Asp
  • NP_001393713.1:p.Glu432Asp
  • NP_001393714.1:p.Glu423Asp
  • NP_001393715.1:p.Glu420Asp
  • NP_001393716.1:p.Glu418Asp
  • NP_001393717.1:p.Glu367Asp
  • NP_001393718.1:p.Glu367Asp
  • NP_001393719.1:p.Glu367Asp
  • NP_001393720.1:p.Glu327Asp
  • NP_001393721.1:p.Glu279Asp
  • NP_001393722.1:p.Glu279Asp
  • NP_001393723.1:p.Glu279Asp
  • NP_065680.1:p.Glu762Asp
  • NP_065681.1:p.Glu762Asp
  • NP_065681.1:p.Glu762Asp
  • NP_065681.1:p.Glu762Asp
  • NP_066124.1:p.Glu762Asp
  • NP_066124.1:p.Glu762Asp
  • LRG_518t1:c.2286G>C
  • LRG_518t2:c.2286G>C
  • LRG_518:g.46306G>C
  • LRG_518p1:p.Glu762Asp
  • LRG_518p2:p.Glu762Asp
  • NC_000010.10:g.43613822G>C
  • NM_001355216.1:c.1524G>C
  • NM_020630.4:c.2286G>C
  • NM_020630.6:c.2286G>C
  • NM_020975.4:c.2286G>C
Protein change:
E279D
Links:
dbSNP: rs1323183090
NCBI 1000 Genomes Browser:
rs1323183090
Molecular consequence:
  • NM_000323.2:c.2286G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001355216.2:c.1524G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406743.1:c.2286G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406744.1:c.2286G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406759.1:c.2286G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406760.1:c.2286G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406761.1:c.2157G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406762.1:c.2157G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406763.1:c.2151G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406764.1:c.2157G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406765.1:c.2151G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406766.1:c.1998G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406767.1:c.1998G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406768.1:c.2022G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406769.1:c.1890G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406770.1:c.1998G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406771.1:c.1848G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406772.1:c.1890G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406773.1:c.1848G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406774.1:c.1761G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406775.1:c.1560G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406776.1:c.1560G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406777.1:c.1560G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406778.1:c.1560G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406779.1:c.1389G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406780.1:c.1389G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406781.1:c.1389G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406782.1:c.1389G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406783.1:c.1260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406784.1:c.1296G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406785.1:c.1269G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406786.1:c.1260G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406787.1:c.1254G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406788.1:c.1101G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406789.1:c.1101G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406790.1:c.1101G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406791.1:c.981G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406792.1:c.837G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406793.1:c.837G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001406794.1:c.837G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_020629.2:c.2286G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_020630.7:c.2286G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_020975.6:c.2286G>C - missense variant - [Sequence Ontology: SO:0001583]
Observations:
1

Condition(s)

Name:
Hereditary cancer-predisposing syndrome
Synonyms:
Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001175858Ambry Genetics
criteria provided, single submitter

(Ambry General Variant Classification Scheme_2022)		Uncertain significance
(Jul 27, 2021) 		germlineclinical testing

Citation Link

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknown1not providednot provided1not providedclinical testing

Details of each submission

From Ambry Genetics, SCV001175858.3

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testingnot provided

Description

The p.E762D variant (also known as c.2286G>C), located in coding exon 13 of the RET gene, results from a G to C substitution at nucleotide position 2286. The glutamic acid at codon 762 is replaced by aspartic acid, an amino acid with highly similar properties. This amino acid position is well conserved in available vertebrate species. In addition, the in silico prediction for this alteration is inconclusive. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknown1not providednot provided1not providednot providednot provided

Last Updated: Apr 20, 2024