Varaico: Literature-Extracted Genetic Variants

Gene:HTT
Variant:p.P42P
Back to variants list

HTT

NM_002111.8:p.P42P

Associated Papers

The frequency and clinical impact of synonymous HTT loss-of-interruption and duplication-of-interruption variants in a diverse HD cohort.

Dawson J et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2024

Chromothripsis 18 in multiple myeloma patient with rapid extramedullary relapse.

Smetana J et al.

Molecular Cytogenetics, 2018

29375670 (PubMed )
Supplement: 13039_2018_357_MOESM2_ESM.xlsx › variants

The genetic landscape of benign thyroid nodules revealed by whole exome and transcriptome sequencing.

Ye L et al.

Nature Communications, 2017

28580939 (PubMed )
Supplement: ncomms15533-s4.xlsx › mutation_list

Co-existence of BRAF and NRAS driver mutations in the same melanoma cells results in heterogeneity of targeted therapy resistance.

Raaijmakers MI et al.

Oncotarget, 2016

27791198 (PubMed )
Supplement: oncotarget-07-77163-s002.xlsx › Patient_2_late_met_2
Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."