SI c.4445T>C ;(p.I1482T)

Variant ID: 3-164716423-A-G

NM_001041.3(SI):c.4445T>C;(p.I1482T)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Significance of rare variants in genes involved in the pathogenesis of Lynch syndrome.

International Journal Of Molecular Medicine
Liccardo, Raffaella R; Lambiase, Matilde M; Nolano, Antonio A; De Rosa, Marina M; Izzo, Paola P; Duraturo, Francesca F
Publication Date: 2022-06

Variant appearance in text: SI: 4445T>C; Ile1482Thr
PubMed Link: 35475445
Variant Present in the following documents:
  • ijmm-49-06-05137.pdf
View BVdb publication page