PC c.338C>A ;(p.A113E)

Variant ID: 11-66638935-G-T

NM_001040716.1(PC):c.338C>A;(p.A113E)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Mismatch repair deficiency in early-onset duodenal, ampullary, and pancreatic carcinomas is a strong indicator for a hereditary defect.

The Journal Of Pathology. Clinical Research
Kryklyva, Valentyna V; Brosens, Lodewijk Aa LA; Marijnissen-van Zanten, Monica Aj MA; Ligtenberg, Marjolijn Jl MJ; Nagtegaal, Iris D ID
Publication Date: 2022-03

Variant appearance in text: PC: 338C>A
PubMed Link: 34873870
Variant Present in the following documents:
  • CJP2-8-181.pdf
View BVdb publication page



Mismatch repair deficiency in early-onset duodenal, ampullary, and pancreatic carcinomas is a strong indicator for a hereditary defect.

The Journal Of Pathology. Clinical Research
Kryklyva, Valentyna V; Brosens, Lodewijk Aa LA; Marijnissen-van Zanten, Monica Aj MA; Ligtenberg, Marjolijn Jl MJ; Nagtegaal, Iris D ID
Publication Date: 2021-12-06

Variant appearance in text: PC: 338C>A
PubMed Link: 34873870
Variant Present in the following documents:
  • CJP2-8-181.pdf
View BVdb publication page



Convergent evolution of tertiary structure in rhodopsin visual proteins from vertebrates and box jellyfish.

Proceedings Of The National Academy Of Sciences Of The United States Of America
Gerrard, Elliot E; Mutt, Eshita E; Nagata, Takashi T; Koyanagi, Mitsumasa M; Flock, Tilman T; Lesca, Elena E; Schertler, Gebhard F X GFX; Terakita, Akihisa A; Deupi, Xavier X; Lucas, Robert J RJ
Publication Date: 2018-06-12

Variant appearance in text: PC: A113E
PubMed Link: 29793939
Variant Present in the following documents:
  • pnas.201721333.pdf
View BVdb publication page