Variant ID: 8-6358293-T-C

NM_001147.2(ANGPT2):c.*2329A>G

This variant was identified in 3 publications



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Genetic variation implicates plasma angiopoietin-2 in the development of acute kidney injury sub-phenotypes.

Bmc Nephrology
PK Bhatraju, M Cohen, RJ Nagao, ED Morrell, S Kosamo, XY Chai, R Nance, V Dmyterko, J Delaney, JD Christie, KD Liu, C Mikacenic, SA Gharib, WC Liles, Y Zheng, DC Christiani, J Himmelfarb, MM Wurfel
Publication Date: 2020-07-17

Variant appearance in text: rs2442473
PubMed Link: 32680471
PubMed Central Link
Variant Present in the following documents:
  • Main text
View BVdb publication page


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: rs2442473
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: rs2442473
PubMed Link: 27015561
PubMed Central Link
Variant Present in the following documents:
  • oncotarget-07-19171-s004.xlsx
View BVdb publication page


Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000325203.5 c.*2329A>G - 3_prime_UTR_variant 9/9 -
ENST00000344683.5 c.2214+843T>C - intron_variant - 12/13
ENST00000415216.1 c.*2329A>G - 3_prime_UTR_variant 9/9 -
ENST00000519221.1 n.321+843T>C - intron_variant,non_coding_transcript_variant - 4/4
ENST00000521129.1 n.372+843T>C - intron_variant,non_coding_transcript_variant - 4/4
NM_001118887.2 c.*2329A>G - 3_prime_UTR_variant 9/9 -
NM_001118888.2 c.*2329A>G - 3_prime_UTR_variant 8/8 -
NM_001147.3 c.*2329A>G - 3_prime_UTR_variant 9/9 -
NM_001322042.2 c.2214+843T>C - intron_variant - 12/14
NM_001363979.1 c.2214+843T>C - intron_variant - 12/13
NM_001363980.2 c.1935+45520T>C - intron_variant - 9/10
NM_024596.5 c.2214+843T>C - intron_variant - 12/13