SI c.1732T>G ;(p.F578V)

Variant ID: 3-164764784-A-C

NM_001041.3(SI):c.1732T>G;(p.F578V)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Heterozygous colon cancer-associated mutations of SAMHD1 have functional significance.

Proceedings Of The National Academy Of Sciences Of The United States Of America
Rentoft, Matilda M; Lindell, Kristoffer K; Tran, Phong P; Chabes, Anna Lena AL; Buckland, Robert J RJ; Watt, Danielle L DL; Marjavaara, Lisette L; Nilsson, Anna Karin AK; Melin, Beatrice B; Trygg, Johan J; Johansson, Erik E; Chabes, Andrei A
Publication Date: 2016-04-26

Variant appearance in text: SI: F578V
PubMed Link: 27071091
Variant Present in the following documents:
  • Main text
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