ACVR2A c.*2218A>T

Variant ID: 2-148687061-A-T

NM_001616.4(ACVR2A):c.*2218A>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genetic analysis of sinonasal undifferentiated carcinoma discovers recurrent SWI/SNF alterations and a novel PGAP3-SRPK1 fusion gene.

Bmc Cancer
Heft Neal, Molly E ME; Birkeland, Andrew C AC; Bhangale, Apurva D AD; Zhai, Jingyi J; Kulkarni, Aditi A; Foltin, Susan K SK; Jewell, Brittany M BM; Ludwig, Megan L ML; Pinatti, Lisa L; Jiang, Hui H; McHugh, Jonathan B JB; Marentette, Lawence L; McKean, Erin L EL; Brenner, J Chad JC
Publication Date: 2021-05-29

Variant appearance in text: rs13430086
PubMed Link: 34051734
Variant Present in the following documents:
  • 12885_2021_8370_MOESM15_ESM.xlsx, sheet 1
View BVdb publication page



Genetic association of the activin A receptor gene (ACVR2A) and pre-eclampsia.

Molecular Human Reproduction
Fitzpatrick, E E; Johnson, M P MP; Dyer, T D TD; Forrest, S S; Elliott, K K; Blangero, J J; Brennecke, S P SP; Moses, E K EK
Publication Date: 2009-03

Variant appearance in text: rs13430086
PubMed Link: 19126782
Variant Present in the following documents:
  • Main text
View BVdb publication page