NM_177438.3(DICER1):c.3770T>C (p.Val1257Ala) AND DICER1-related tumor predisposition

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jun 7, 2022
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:: RCV002820538.3

Allele description [Variation Report for NM_177438.3(DICER1):c.3770T>C (p.Val1257Ala)]

NM_177438.3(DICER1):c.3770T>C (p.Val1257Ala)

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.3770T>C (p.Val1257Ala)

HGVS:

NC_000014.9:g.95103626A>G
NG_016311.1:g.58797T>C
NM_001195573.1:c.3770T>C
NM_001271282.3:c.3770T>C
NM_001291628.2:c.3770T>C
NM_001395677.1:c.3770T>C
NM_001395678.1:c.3770T>C
NM_001395679.1:c.3770T>C
NM_001395680.1:c.3770T>C
NM_001395681.1:c.3770T>C
NM_001395682.1:c.3770T>C
NM_001395683.1:c.3770T>C
NM_001395684.1:c.3770T>C
NM_001395686.1:c.3488T>C
NM_001395687.1:c.3365T>C
NM_001395688.1:c.3365T>C
NM_001395689.1:c.3365T>C
NM_001395690.1:c.3365T>C
NM_001395691.1:c.3203T>C
NM_001395692.1:c.3770T>C
NM_001395693.1:c.3770T>C
NM_001395694.1:c.3770T>C
NM_001395695.1:c.3770T>C
NM_001395696.1:c.3365T>C
NM_001395697.1:c.2087T>C
NM_030621.4:c.3770T>C
NM_177438.3:c.3770T>CMANE SELECT
NP_001182502.1:p.Val1257Ala
NP_001258211.1:p.Val1257Ala
NP_001278557.1:p.Val1257Ala
NP_001382606.1:p.Val1257Ala
NP_001382607.1:p.Val1257Ala
NP_001382608.1:p.Val1257Ala
NP_001382609.1:p.Val1257Ala
NP_001382610.1:p.Val1257Ala
NP_001382611.1:p.Val1257Ala
NP_001382612.1:p.Val1257Ala
NP_001382613.1:p.Val1257Ala
NP_001382615.1:p.Val1163Ala
NP_001382616.1:p.Val1122Ala
NP_001382617.1:p.Val1122Ala
NP_001382618.1:p.Val1122Ala
NP_001382619.1:p.Val1122Ala
NP_001382620.1:p.Val1068Ala
NP_001382621.1:p.Val1257Ala
NP_001382622.1:p.Val1257Ala
NP_001382623.1:p.Val1257Ala
NP_001382624.1:p.Val1257Ala
NP_001382625.1:p.Val1122Ala
NP_001382626.1:p.Val696Ala
NP_085124.2:p.Val1257Ala
NP_803187.1:p.Val1257Ala
NP_803187.1:p.Val1257Ala
LRG_492t1:c.3770T>C
LRG_492:g.58797T>C
LRG_492p1:p.Val1257Ala
NC_000014.8:g.95569963A>G
NM_177438.2:c.3770T>C
NR_172715.1:n.4188T>C
NR_172716.1:n.4372T>C
NR_172717.1:n.4282T>C
NR_172718.1:n.4205T>C
NR_172719.1:n.4038T>C
NR_172720.1:n.4115T>C

Protein change:

V1068A

Molecular consequence:

NM_001195573.1:c.3770T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001271282.3:c.3770T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001291628.2:c.3770T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001395677.1:c.3770T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001395678.1:c.3770T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001395679.1:c.3770T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001395680.1:c.3770T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001395681.1:c.3770T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001395682.1:c.3770T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001395683.1:c.3770T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001395684.1:c.3770T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001395686.1:c.3488T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001395687.1:c.3365T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001395688.1:c.3365T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001395689.1:c.3365T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001395690.1:c.3365T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001395691.1:c.3203T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001395692.1:c.3770T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001395693.1:c.3770T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001395694.1:c.3770T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001395695.1:c.3770T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001395696.1:c.3365T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001395697.1:c.2087T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_030621.4:c.3770T>C - missense variant - [Sequence Ontology: SO:0001583]
NM_177438.3:c.3770T>C - missense variant - [Sequence Ontology: SO:0001583]
NR_172715.1:n.4188T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_172716.1:n.4372T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_172717.1:n.4282T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_172718.1:n.4205T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_172719.1:n.4038T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_172720.1:n.4115T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]

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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Gene ID:856009

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003207332	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Jun 7, 2022)	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

SCV003207332

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Jun 7, 2022)

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, SCV003207332.2

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

Description

This sequence change replaces valine, which is neutral and non-polar, with alanine, which is neutral and non-polar, at codon 1257 of the DICER1 protein (p.Val1257Ala). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with DICER1-related conditions. Algorithms developed to predict the effect of missense changes on protein structure and function output the following: SIFT: "Tolerated"; PolyPhen-2: "Benign"; Align-GVGD: "Class C0". The alanine amino acid residue is found in multiple mammalian species, which suggests that this missense change does not adversely affect protein function. 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.

#	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: Oct 8, 2024

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