Variant ID: 8-6395909-G-T

NM_001147.2(ANGPT2):c.289-5901C>A

This variant was identified in 7 publications




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: rs11989215
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



MicroRNA signatures in vitreous humour and plasma of patients with exudative AMD.

Oncotarget
C Ménard, FA Rezende, K Miloudi, A Wilson, N Tétreault, P Hardy, JP SanGiovanni, V De Guire, P Sapieha
Publication Date: 2016-04-12

Variant appearance in text: rs11989215
PubMed Link: 27015561
PubMed Central Link
Variant Present in the following documents:
  • oncotarget-07-19171-s004.xlsx
View BVdb publication page



Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND).

Plos Genetics
SK Iyengar, JR Sedor, BI Freedman, WH Kao, M Kretzler, BJ Keller, HE Abboud, SG Adler, LG Best, DW Bowden, A Burlock, YD Chen, SA Cole, ME Comeau, JM Curtis, J Divers, C Drechsler, R Duggirala, RC Elston, X Guo, H Huang, MM Hoffmann, BV Howard, E Ipp, PL Kimmel, MJ Klag, WC Knowler, OF Kohn, TS Leak, DJ Leehey, M Li, A Malhotra, W März, V Nair, RG Nelson, SB Nicholas, SJ O'Brien, MV Pahl, RS Parekh, MG Pezzolesi, RS Rasooly, CN Rotimi, JI Rotter, JR Schelling, MF Seldin, VO Shah, AM Smiles, MW Smith, KD Taylor, F Thameem, DP Thornley-Brown, BJ Truitt, C Wanner, EJ Weil, CA Winkler, PG Zager, RP Igo, RL Hanson, CD Langefeld,
Publication Date: 2015-08

Variant appearance in text: rs11989215
PubMed Link: 26305897
PubMed Central Link
Variant Present in the following documents:
  • pgen.1005352.s004.docx
View BVdb publication page



The International SSRI Pharmacogenomics Consortium (ISPC): a genome-wide association study of antidepressant treatment response.

Translational Psychiatry
JM Biernacka, K Sangkuhl, G Jenkins, RM Whaley, P Barman, A Batzler, RB Altman, V Arolt, J Brockmöller, CH Chen, K Domschke, DK Hall-Flavin, CJ Hong, A Illi, Y Ji, O Kampman, T Kinoshita, E Leinonen, YJ Liou, T Mushiroda, S Nonen, MK Skime, L Wang, BT Baune, M Kato, YL Liu, V Praphanphoj, JC Stingl, SJ Tsai, M Kubo, TE Klein, R Weinshilboum
Publication Date: 2015-04-21

Variant appearance in text: rs11989215
PubMed Link: 25897834
PubMed Central Link
Variant Present in the following documents:
  • Main text
  • tp201547x1.docx
View BVdb publication page



Genetics of common forms of heart failure: challenges and potential solutions.

Current Opinion In Cardiology
CD Rau, AJ Lusis, Y Wang
Publication Date: 2015-05

Variant appearance in text: rs11989215
PubMed Link: 25768955
PubMed Central Link
Variant Present in the following documents:
  • NIHMS678829-supplement-Supplemental_Digital_Content_2.docx
View BVdb publication page



Lymphatic and angiogenic candidate genes predict the development of secondary lymphedema following breast cancer surgery.

Plos One
C Miaskowski, M Dodd, SM Paul, C West, D Hamolsky, G Abrams, BA Cooper, C Elboim, J Neuhaus, BL Schmidt, B Smoot, BE Aouizerat
Publication Date: 2013

Variant appearance in text: rs11989215
PubMed Link: 23613720
PubMed Central Link
Variant Present in the following documents:
  • Main text
View BVdb publication page



Common variants in HSPB7 and FRMD4B associated with advanced heart failure.

Circulation. Cardiovascular Genetics
TP Cappola, M Li, J He, B Ky, J Gilmore, L Qu, B Keating, M Reilly, CE Kim, J Glessner, E Frackelton, H Hakonarson, F Syed, A Hindes, SJ Matkovich, S Cresci, GW Dorn
Publication Date: 2010-04

Variant appearance in text: rs11989215
PubMed Link: 20124441
PubMed Central Link
Variant Present in the following documents:
  • NIHMS238368-supplement-Supplement.pdf
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000325203.5 c.289-5901C>A - intron_variant - 1/8
ENST00000338312.6 c.289-10712C>A - intron_variant - 1/7
ENST00000344683.5 c.2214+38459G>T - intron_variant - 12/13
ENST00000415216.1 c.289-5901C>A - intron_variant - 1/8
ENST00000519221.1 n.321+38459G>T - intron_variant,non_coding_transcript_variant - 4/4
ENST00000521129.1 n.372+38459G>T - intron_variant,non_coding_transcript_variant - 4/4
ENST00000523120.1 c.289-5901C>A - intron_variant - 1/7
NM_001118887.2 c.289-5901C>A - intron_variant - 1/8
NM_001118888.2 c.289-10712C>A - intron_variant - 1/7
NM_001147.3 c.289-5901C>A - intron_variant - 1/8
NM_001322042.2 c.2214+38459G>T - intron_variant - 12/14
NM_001363979.1 c.2214+38459G>T - intron_variant - 12/13
NM_001363980.2 c.1936-83066G>T - intron_variant - 9/10
NM_024596.5 c.2214+38459G>T - intron_variant - 12/13