Bibliome.ai browser hg19
Search
About
Stats
FAQ
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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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