Clonal hematopoiesis as a pitfall in germline variant interpretation in the context of Mendelian disorders. Issue 14 (18th February 2022)
- Record Type:
- Journal Article
- Title:
- Clonal hematopoiesis as a pitfall in germline variant interpretation in the context of Mendelian disorders. Issue 14 (18th February 2022)
- Main Title:
- Clonal hematopoiesis as a pitfall in germline variant interpretation in the context of Mendelian disorders
- Authors:
- Brunet, Theresa
Berutti, Riccardo
Dill, Veronika
Hecker, Judith S
Choukair, Daniela
Andres, Stephanie
Deschauer, Marcus
Diehl-Schmid, Janine
Krenn, Martin
Eckstein, Gertrud
Graf, Elisabeth
Gasser, Thomas
Strom, Tim M
Hoefele, Julia
Götze, Katharina S
Meitinger, Thomas
Wagner, Matias - Abstract:
- Abstract: Clonal hematopoiesis because of somatic mutations in hematopoietic stem/progenitor cells is an age-related phenomenon and commonly observed when sequencing blood DNA in elderly individuals. Several genes that are implicated in clonal hematopoiesis are also associated with Mendelian disorders when mutated in the germline, potentially leading to variant misinterpretation. We performed a literature search to identify genes associated with age-related clonal hematopoiesis followed by an OMIM query to identify the subset of genes in which germline variants are associated with Mendelian disorders. We retrospectively screened for diagnostic cases in which the presence of age-related clonal hematopoiesis confounded exome sequencing data interpretation. We found 58 genes in which somatic mutations are implicated in clonal hematopoiesis, while germline variants in the same genes are associated with Mendelian (mostly neurodevelopmental) disorders. Using five selected cases of individuals with suspected monogenic disorders, we illustrate how clonal hematopoiesis in either variant databases or exome sequencing datasets poses a pitfall, potentially leading to variant misclassification and erroneous conclusions regarding gene–disease associations.
- Is Part Of:
- Human molecular genetics. Volume 31:Issue 14(2022)
- Journal:
- Human molecular genetics
- Issue:
- Volume 31:Issue 14(2022)
- Issue Display:
- Volume 31, Issue 14 (2022)
- Year:
- 2022
- Volume:
- 31
- Issue:
- 14
- Issue Sort Value:
- 2022-0031-0014-0000
- Page Start:
- 2386
- Page End:
- 2395
- Publication Date:
- 2022-02-18
- Subjects:
- Human molecular genetics -- Periodicals
Human chromosome abnormalities -- Periodicals
572.8 - Journal URLs:
- http://hmg.oxfordjournals.org/ ↗
http://ukcatalogue.oup.com/ ↗ - DOI:
- 10.1093/hmg/ddac034 ↗
- Languages:
- English
- ISSNs:
- 0964-6906
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4336.198000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 22591.xml