Variant ID: 9-27206307-A-C


This variant was identified in 2 publications


Germline Genetic Variants in TEK, ANGPT1, ANGPT2, MMP9, FGF2 and VEGFA Are Associated with Pathologic Complete Response to Bevacizumab in Breast Cancer Patients.

Plos One
I Makhoul, VK Todorova, ER Siegel, SW Erickson, I Dhakal, VR Raj, JY Lee, MS Orloff, RJ Griffin, RS Henry-Tillman, S Klimberg, LF Hutchins, SA Kadlubar
Publication Date: 2017

Variant appearance in text: rs510101
PubMed Link: 28045923
PubMed Central Link
Variant Present in the following documents:
  • pone.0168550.s011.xlsx
  • pone.0168550.s006.xlsx
  • pone.0168550.s007.xlsx
  • pone.0168550.s004.xlsx
  • pone.0168550.s009.xlsx
  • pone.0168550.s005.xlsx
  • pone.0168550.s003.xlsx
View BVdb publication page

Assessment of hepatocyte growth factor in ovarian cancer mortality.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
EL Goode, G Chenevix-Trench, LC Hartmann, BL Fridley, KR Kalli, RA Vierkant, MC Larson, KL White, GL Keeney, TN Oberg, JM Cunningham, J Beesley, SE Johnatty, X Chen, KE Goodman, SM Armasu, DN Rider, H Sicotte, MM Schmidt, EA Elliott, E Høgdall, SK Kjær, PA Fasching, AB Ekici, D Lambrechts, E Despierre, C Høgdall, L Lundvall, BY Karlan, J Gross, R Brown, J Chien, DJ Duggan, YY Tsai, CM Phelan, LE Kelemen, PP Peethambaram, JM Schildkraut, V Shridhar, R Sutphen, FJ Couch, TA Sellers,
Publication Date: 2011-08

Variant appearance in text: rs510101
PubMed Link: 21724856
PubMed Central Link
Variant Present in the following documents:
  • NIHMS308552-supplement-1.xls
View BVdb publication page

Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000380036.4 c.2365-273A>C - intron_variant - 14/22
ENST00000406359.4 c.2236-273A>C - intron_variant - 13/21
ENST00000519097.1 c.1921-273A>C - intron_variant - 12/20
NM_000459.4 c.2365-273A>C - intron_variant - 14/22
NM_001290077.1 c.2236-273A>C - intron_variant - 13/21
NM_001290078.1 c.1921-273A>C - intron_variant - 12/20