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Article

HLA-C locus allelic dropout in Sanger sequence-based typing due to intronic single nucleotide polymorphism.

Human immunology - 1 Dec 2014

Cheng Christopher, Kashi Zahra Mehdizadeh, Martin Russell, Woodruff Gillian, Dinauer David, Agostini Tina

Abstract excerpt

We report a novel HLA-C allele that was identified during routine HLA typing using sequence-based methods. The patient was initially typed as a C*06:02, 06:04 with two nucleotide mismatches in exon 3, (C to T and T to G changes) which would have resulted in a non-synonymous mutation of a leucine...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Leukemia, Myeloid, Acute

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Share to Polymorphism, Single Nucleotide

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Source

Identifiers

PMID: 25315749
DOI: 10.1016/j.humimm.2014.09.016

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-25315749-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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