NM_177438.3(DICER1):c.5471G>A (p.Gly1824Glu) AND DICER1-related tumor predisposition

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Sep 20, 2023
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:: RCV000802123.9

Allele description [Variation Report for NM_177438.3(DICER1):c.5471G>A (p.Gly1824Glu)]

NM_177438.3(DICER1):c.5471G>A (p.Gly1824Glu)

Gene:

DICER1:dicer 1, ribonuclease III [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

14q32.13

Genomic location:

Preferred name:

NM_177438.3(DICER1):c.5471G>A (p.Gly1824Glu)

HGVS:

NC_000014.9:g.95091259C>T
NG_016311.1:g.71164G>A
NM_001195573.1:c.5365-150G>A
NM_001271282.3:c.5471G>A
NM_001291628.2:c.5471G>A
NM_030621.4:c.5471G>A
NM_177438.3:c.5471G>AMANE SELECT
NP_001258211.1:p.Gly1824Glu
NP_001278557.1:p.Gly1824Glu
NP_085124.2:p.Gly1824Glu
NP_803187.1:p.Gly1824Glu
NP_803187.1:p.Gly1824Glu
LRG_492t1:c.5471G>A
LRG_492:g.71164G>A
LRG_492p1:p.Gly1824Glu
NC_000014.8:g.95557596C>T
NM_177438.2:c.5471G>A

Protein change:

G1824E

Links:

dbSNP: rs377685186

NCBI 1000 Genomes Browser:

rs377685186

Molecular consequence:

NM_001195573.1:c.5365-150G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001271282.3:c.5471G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001291628.2:c.5471G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_030621.4:c.5471G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_177438.3:c.5471G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: DICER1-related tumor predisposition
Synonyms:: DICER1-related pleuropulmonary blastoma cancer predisposition syndrome; DICER1 syndrome
Identifiers:: MONDO: MONDO:0100216; MedGen: C3839822

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000941939	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Sep 20, 2023)	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

SCV000941939

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Sep 20, 2023)

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

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, SCV000941939.6

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

Description

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. An algorithm developed to predict the effect of missense changes on protein structure and function (PolyPhen-2) suggests that this variant¬†is likely to be tolerated. ClinVar contains an entry for this variant (Variation ID: 647583). This variant has not been reported in the literature in individuals affected with DICER1-related conditions. This variant is not present in population databases (gnomAD no frequency). This sequence change replaces glycine, which is neutral and non-polar, with glutamic acid, which is acidic and polar, at codon 1824 of the DICER1 protein (p.Gly1824Glu).

#	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: Nov 18, 2024

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