APC c.2684C>T ;(p.S895L)

Variant ID: 5-112173975-C-T

NM_000038.5(APC):c.2684C>T;(p.S895L)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Genetic heterogeneity in hepatocellular carcinoma and paired bone metastasis revealed by next-generation sequencing.

International Journal Of Clinical And Experimental Pathology
Jin, Ketao K; Lan, Huanrong H; Wang, Xuanwei X; Lv, Jieqing J
Publication Date: 2017

Variant appearance in text: APC: 2684C>T; Ser895Leu
PubMed Link: 31966388
Variant Present in the following documents:
  • Main text
View BVdb publication page



Distinctive DNA mismatch repair and APC rare variants in African Americans with colorectal neoplasia.

Oncotarget
Ashktorab, Hassan H; Azimi, Hamed H; Varma, Sudhir S; Tavakoli, Payaam P; Nickerson, Michael L ML; Brim, Hassan H
Publication Date: 2017-11-21

Variant appearance in text: APC: S895L
PubMed Link: 29245953
Variant Present in the following documents:
  • oncotarget-08-99966-s003.xlsx, sheet 3
View BVdb publication page



Targeted next-generation sequencing of cancer genes in poorly differentiated thyroid cancer.

Endocrine Connections
Gerber, Tiemo S TS; Schad, Arno A; Hartmann, Nils N; Springer, Erik E; Zechner, Ulrich U; Musholt, Thomas J TJ
Publication Date: 2018-01

Variant appearance in text: APC: 2684C>T
PubMed Link: 29133385
Variant Present in the following documents:
  • ec-7-47-t001.pdf
View BVdb publication page