SMARCA4 c.1156_1157del ;(p.E386Kfs*17)

Variant ID: 19-11100030-TGA-T

NM_003072.3(SMARCA4):c.1156_1157del;(p.E386Kfs*17)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Diagnostic Yield of Clinical Tumor and Germline Whole-Exome Sequencing for Children With Solid Tumors.

Jama Oncology
Parsons, D Williams DW; Roy, Angshumoy A; Yang, Yaping Y; Wang, Tao T; Scollon, Sarah S; Bergstrom, Katie K; Kerstein, Robin A RA; Gutierrez, Stephanie S; Petersen, Andrea K AK; Bavle, Abhishek A; Lin, Frank Y FY; López-Terrada, Dolores H DH; Monzon, Federico A FA; Hicks, M John MJ; Eldin, Karen W KW; Quintanilla, Norma M NM; Adesina, Adekunle M AM; Mohila, Carrie A CA; Whitehead, William W; Jea, Andrew A; Vasudevan, Sanjeev A SA; Nuchtern, Jed G JG; Ramamurthy, Uma U; McGuire, Amy L AL; Hilsenbeck, Susan G SG; Reid, Jeffrey G JG; Muzny, Donna M DM; Wheeler, David A DA; Berg, Stacey L SL; Chintagumpala, Murali M MM; Eng, Christine M CM; Gibbs, Richard A RA; Plon, Sharon E SE
Publication Date: 2016-05-01

Variant appearance in text: SMARCA4: 1156_1157del; E386fs
PubMed Link: 26822237
Variant Present in the following documents:
  • Main text
View BVdb publication page