HMCN1 c.10238G>T ;(p.C3413F)

Variant ID: 1-186063449-G-T

NM_031935.2(HMCN1):c.10238G>T;(p.C3413F)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genetic alterations associated with progression from pancreatic intraepithelial neoplasia to invasive pancreatic tumor.

Gastroenterology
Murphy, Stephen J SJ; Hart, Steven N SN; Lima, Joema Felipe JF; Kipp, Benjamin R BR; Klebig, Mitchell M; Winters, Jennifer L JL; Szabo, Csilla C; Zhang, Lizhi L; Eckloff, Bruce W BW; Petersen, Gloria M GM; Scherer, Steven E SE; Gibbs, Richard A RA; McWilliams, Robert R RR; Vasmatzis, George G; Couch, Fergus J FJ
Publication Date: 2013-11

Variant appearance in text: HMCN1: C3413F
PubMed Link: 23912084
Variant Present in the following documents:
  • Main text
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