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NM_152383.5(DIS3L2):c.79G>C (p.Asp27His) AND Perlman syndrome

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jul 16, 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:
RCV000535106.10

Allele description [Variation Report for NM_152383.5(DIS3L2):c.79G>C (p.Asp27His)]

NM_152383.5(DIS3L2):c.79G>C (p.Asp27His)

Gene:
DIS3L2:DIS3 like 3'-5' exoribonuclease 2 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
2q37.1
Genomic location:
Preferred name:
NM_152383.5(DIS3L2):c.79G>C (p.Asp27His)
HGVS:
  • NC_000002.12:g.232015540G>C
  • NG_032572.1:g.58958G>C
  • NM_001257281.2:c.79G>C
  • NM_001257282.2:c.79G>C
  • NM_152383.5:c.79G>CMANE SELECT
  • NP_001244210.1:p.Asp27His
  • NP_001244211.1:p.Asp27His
  • NP_689596.4:p.Asp27His
  • NP_689596.4:p.Asp27His
  • LRG_534t1:c.79G>C
  • LRG_534:g.58958G>C
  • LRG_534p1:p.Asp27His
  • NC_000002.11:g.232880250G>C
  • NM_152383.4:c.79G>C
  • NR_046476.2:n.225G>C
  • NR_046477.2:n.225G>C
Protein change:
D27H
Links:
dbSNP: rs780747005
NCBI 1000 Genomes Browser:
rs780747005
Molecular consequence:
  • NM_001257281.2:c.79G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001257282.2:c.79G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_152383.5:c.79G>C - missense variant - [Sequence Ontology: SO:0001583]
  • NR_046476.2:n.225G>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_046477.2:n.225G>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:
Perlman syndrome (PRLMNS)
Synonyms:
Renal hamartomas nephroblastomatosis and fetal gigantism; Nephroblastomatosis fetal ascites macrosomia and wilms tumor
Identifiers:
MONDO: MONDO:0009965; MedGen: C0796113; Orphanet: 2849; OMIM: 267000

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000636803Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(Jul 16, 2023) 		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, SCV000636803.8

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

Description

This sequence change replaces aspartic acid, which is acidic and polar, with histidine, which is basic and polar, at codon 27 of the DIS3L2 protein (p.Asp27His). This variant is present in population databases (rs780747005, gnomAD 0.003%). This variant has not been reported in the literature in individuals affected with DIS3L2-related conditions. ClinVar contains an entry for this variant (Variation ID: 463130). 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. 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: Sep 29, 2024