ATM c.5385G>T ;(p.W1795C)

Variant ID: 11-108173645-G-T

NM_000051.3(ATM):c.5385G>T;(p.W1795C)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Combinations of Low-Frequency Genetic Variants Might Predispose to Familial Pancreatic Cancer.

Journal Of Personalized Medicine
Slater, Emily P EP; Wilke, Lisa M LM; Böhm, Lutz Benedikt LB; Strauch, Konstantin K; Lutz, Manuel M; Gercke, Norman N; Matthäi, Elvira E; Hemminki, Kari K; Försti, Asta A; Schlesner, Matthias M; Paramasivam, Nagarajan N; Bartsch, Detlef K DK
Publication Date: 2021-07-02

Variant appearance in text: ATM: 5385G>T; W1795C
PubMed Link: 34357098
Variant Present in the following documents:
  • Main text
  • jpm-11-00631.pdf
View BVdb publication page