142: PALB2 ACMG/AMP Specifications
Base by Base19 Sep 2025

142: PALB2 ACMG/AMP Specifications

Richardson M et al., The American Journal of Human Genetics - An international HBOP Variant Curation Expert Panel developed PALB2-specific specifications of the 2015 ACMG/AMP variant-interpretation guidelines by tailoring, limiting, or removing existing codes and tested them on 39 pilot variants to improve ClinVar concordance and harmonize classification. Key terms: PALB2, ACMG/AMP, variant curation, HBOP VCEP, ClinVar.

Study Highlights:
The HBOP VCEP reviewed ACMG/AMP codes and advised against 13 codes, limited six, and tailored nine to PALB2-specific biology. They set conservative population thresholds (BA1 0.1%, BS1 0.01%) and refined PVS1/PVS1(RNA) application, defining Tyr1183 as a C-terminal boundary for loss-of-function evidence. A pilot curation of 39 variants produced concordant classifications for 31 of 37 ClinVar variants (84%) and led to reclassification of several VUS/conflicting entries. The recommendations are conservative and evidence-based to support harmonized PALB2 variant interpretation and clinical reporting.

Conclusion:
PALB2-specific ACMG/AMP specifications provide a conservative, evidence-based framework that improves harmonization and accuracy of variant classification, supporting ClinVar deposition and clinical management of carriers.

Music:
Enjoy the music based on this article at the end of the episode.

Article title:
Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline PALB2 sequence variants

First author:
Richardson M

Journal:
The American Journal of Human Genetics

DOI:
10.1016/j.ajhg.2025.08.020

Reference:
Richardson M.E. et al., Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline PALB2 sequence variants. The American Journal of Human Genetics. 2025;112:1–15. https://doi.org/10.1016/j.ajhg.2025.08.020

License:
This episode is based on an open-access article published under the Creative Commons Attribution 4.0 International License (CC BY 4.0) – https://creativecommons.org/licenses/by/4.0/

Support:
Base by Base – Stripe donations: https://donate.stripe.com/7sY4gz71B2sN3RWac5gEg00

Official website https://basebybase.com

On PaperCast Base by Base you'll discover the latest in genomics, functional genomics, structural genomics, and proteomics.

Episode link: https://basebybase.com/episodes/specifications-of-the-acmg-amp-guidelines-for-palb2-variant-interpretation

QC:
This episode was checked against the original article PDF and publication metadata for the episode release published on 2025-09-19.

QC Scope:
- article metadata and core scientific claims from the narration
- excludes analogies, intro/outro, and music
- transcript coverage: Audited the transcript sections on PALB2 biology, HBOPVCEP PALB2 specifications, ACMG/AMP code modifications, pilot study outcomes, missense/pathogenicity limitations, PVS1/Tyr1183 boundary, splicing guidance, VUS backlog, and the need for high-throughput functional assays.
- transcript topics: PALB2 role in homologous recombination repair; HBOPVCEP PALB2 specifications and code changes; Pilot study results and ClinVar concordance; VUS resolution outcomes; Missense pathogenicity limitations and splicing considerations; PVS1, Tyr1183 boundary and RNA splicing guidance

QC Summary:
- factual score: 10/10
- metadata score: 10/10
- supported core claims: 7
- claims flagged for review: 0
- metadata checks passed: 4
- metadata issues found: 0

Metadata Audited:
- article_doi
- article_title
- article_journal
- license

Factual Items Audited:
- HBOPVCEP PALB2 specifications exist and tailor/limit ACMG/AMP codes for PALB2
- Pilot with 39 PALB2 variants; 37 in ClinVar; 84% concordance with ClinVar classifications
- Among ClinVar VUS/...

Det här avsnittet är hämtat från ett öppet RSS-flöde och publiceras inte av Podme. Det kan innehålla reklam.

Avsnitt(462)

461: Adult Ank3 loss quiets neurons and lowers a myelin protein

461: Adult Ank3 loss quiets neurons and lowers a myelin protein

Yoon et al., Proceedings of the National Academy of Sciences - ANK3, which encodes the scaffolding protein ankyrin-G, is a major risk gene for bipolar disorder and schizophrenia, yet what it does in a...

24 Sep 24min

460: The lupus variant that also sharpens antiviral defense

460: The lupus variant that also sharpens antiviral defense

Virolainen et al., The American Journal of Human Genetics - A lupus signal on chromosome 11p15 narrows to a coding haplotype in IRF7 that most people in the world carry. This study shows the risk form...

21 Sep 24min

459: Cerebral palsy genetics: 515 candidate genes, evidence for 89

459: Cerebral palsy genetics: 515 candidate genes, evidence for 89

Arterbery et al., The American Journal of Human Genetics - Hundreds of genes have been reported as causes of cerebral palsy, yet there is no agreed model of what a pathogenic variant in a child with C...

13 Sep 24min

458: Somatic or inherited? Reading TP53 risk from shared DNA

458: Somatic or inherited? Reading TP53 risk from shared DNA

MacGregor et al., The American Journal of Human Genetics - Pathogenic TP53 variants found in blood have long been read as inherited Li-Fraumeni alleles, but many turn out to be somatic clones that gre...

10 Sep 25min

457: A deletion that raises Alzheimer risk, a duplication that lowers it

457: A deletion that raises Alzheimer risk, a duplication that lowers it

Quenez O et al., The American Journal of Human Genetics - Rare copy-number variants were called from 22,319 exomes covering early-onset Alzheimer disease, late-onset disease and unaffected controls, t...

9 Sep 24min

456: Beyond exons: where heritability hides as traits get more polygenic

456: Beyond exons: where heritability hides as traits get more polygenic

Fuhrer J et al., The American Journal of Human Genetics - Across 34 complex traits and disorders, a MiXeR-based framework partitions SNP heritability over 74 functional annotations and finds that exon...

8 Sep 45min

455: Agentic genomics: the bottleneck moves from code to judgment

455: Agentic genomics: the bottleneck moves from code to judgment

Corpas M et al., Cell Genomics - A Perspective arguing that autonomous AI agents which discover, configure and chain bioinformatics operations from natural-language instructions have shifted the bottl...

7 Sep 13min

454: Efavirenz retarda a doença priônica mexendo no colesterol do cérebro [PT]

454: Efavirenz retarda a doença priônica mexendo no colesterol do cérebro [PT]

Ali T et al., JCI Insight - Um antirretroviral aprovado para HIV, dado por via oral em microdose, prolongou a sobrevida de camundongos que carregam a proteína priônica humana e foram infectados com pr...

2 Sep 17min

Populärt inom Vetenskap

dumma-manniskor
p3-dystopia
rss-mottagningen
allt-du-velat-veta
angestpodden
kapitalet-en-podd-om-ekonomi
rss-ronden
det-morka-psyket
ufo-sverige
svd-nyhetsartiklar
4health-med-anna-sparre
sexet
rss-vetenskapsradion
rss-arkeologi-historia-podden-som-graver-i-vart-kulturlandskap
bildningspodden
rss-spraket
rss-vetenskapsradion-2
ideer-som-forandrar-varlden
rss-ufobortom-rimligt-tvivel
rss-geopodden-2