Variant ID: 4-123773579-T-G

NM_002006.4(FGF2):c.578-23897T>G

This variant was identified in 9 publications



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

Publications:

Growth factor genes and change in mammographic density after stopping combined hormone therapy in the California Teachers Study.

Bmc Cancer
E Lee, J Luo, FR Schumacher, D Van Den Berg, AH Wu, DO Stram, L Bernstein, G Ursin
Publication Date: 2018-11-06

Variant appearance in text: rs308439
PubMed Link: 30400783
PubMed Central Link
Variant Present in the following documents:
  • 12885_2018_4981_MOESM2_ESM.xlsx
View BVdb publication page


Genetic susceptibility to bone and soft tissue sarcomas: a field synopsis and meta-analysis.

Oncotarget
C Benna, A Simioni, S Pasquali, D De Boni, S Rajendran, G Spiro, C Colombo, C Virgone, SG DuBois, A Gronchi, CR Rossi, S Mocellin
Publication Date: 2018-04-06

Variant appearance in text: rs308439
PubMed Link: 29719630
PubMed Central Link
Variant Present in the following documents:
  • oncotarget-09-18607-s002.docx
View BVdb publication page


Genome-wide association study of coronary artery calcified atherosclerotic plaque in African Americans with type 2 diabetes.

Bmc Genetics
J Divers, ND Palmer, CD Langefeld, WM Brown, L Lu, PJ Hicks, SC Smith, J Xu, JG Terry, TC Register, LE Wagenknecht, JS Parks, L Ma, GC Chan, SG Buxbaum, A Correa, S Musani, JG Wilson, HA Taylor, DW Bowden, JJ Carr, BI Freedman
Publication Date: 2017-12-08

Variant appearance in text: rs308439
PubMed Link: 29221444
PubMed Central Link
Variant Present in the following documents:
  • 12863_2017_572_MOESM4_ESM.xlsx
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: rs308439
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


Genetic Basis of Irritant Susceptibility in Health Care Workers.

Journal Of Occupational And Environmental Medicine
B Yucesoy, Y Talzhanov, MM Barmada, VJ Johnson, ML Kashon, E Baron, NW Wilson, B Frye, W Wang, K Fluharty, R Gharib, J Meade, D Germolec, MI Luster, S Nedorost
Publication Date: 2016-08

Variant appearance in text: rs308439
PubMed Link: 27206134
PubMed Central Link
Variant Present in the following documents:
  • Main text
View BVdb publication page


Genome-wide association study identifies two susceptibility loci for osteosarcoma.

Nature Genetics
SA Savage, L Mirabello, Z Wang, JM Gastier-Foster, R Gorlick, C Khanna, AM Flanagan, R Tirabosco, IL Andrulis, JS Wunder, N Gokgoz, A Patiño-Garcia, L Sierrasesúmaga, F Lecanda, N Kurucu, IE Ilhan, N Sari, M Serra, C Hattinger, P Picci, LG Spector, DA Barkauskas, N Marina, SR de Toledo, AS Petrilli, MF Amary, D Halai, DM Thomas, C Douglass, PS Meltzer, K Jacobs, CC Chung, SI Berndt, MP Purdue, NE Caporaso, M Tucker, N Rothman, MT Landi, DT Silverman, P Kraft, DJ Hunter, N Malats, M Kogevinas, S Wacholder, R Troisi, L Helman, JF Fraumeni, M Yeager, RN Hoover, SJ Chanock
Publication Date: 2013-07

Variant appearance in text: rs308439
PubMed Link: 23727862
PubMed Central Link
Variant Present in the following documents:
  • NIHMS474981-supplement-1.pdf
View BVdb publication page


A candidate gene approach to identify modifiers of the palatal phenotype in 22q11.2 deletion syndrome patients.

International Journal Of Pediatric Otorhinolaryngology
JC Widdershoven, M Bowser, MB Sheridan, DM McDonald-McGinn, EH Zackai, CB Solot, RE Kirschner, FA Beemer, BE Morrow, M Devoto, BS Emanuel
Publication Date: 2013-01

Variant appearance in text: rs308439
PubMed Link: 23121717
PubMed Central Link
Variant Present in the following documents:
  • NIHMS501994-supplement-supplemental.pdf
View BVdb publication page


Polymorphisms in the FGF2 gene and risk of serous ovarian cancer: results from the ovarian cancer association consortium.

Twin Research And Human Genetics : The Official Journal Of The International Society For Twin Studies
SE Johnatty, J Beesley, X Chen, AB Spurdle, A Defazio, PM Webb, , , EL Goode, DN Rider, RA Vierkant, S Anderson, AH Wu, M Pike, D Van Den Berg, K Moysich, R Ness, J Doherty, MA Rossing, CL Pearce, G Chenevix-Trench
Publication Date: 2009-06

Variant appearance in text: rs308439
PubMed Link: 19456219
PubMed Central Link
Variant Present in the following documents:
  • Main text
View BVdb publication page


Common variation in genes related to innate immunity and risk of adult glioma.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
P Rajaraman, AV Brenner, MA Butler, SS Wang, RM Pfeiffer, AM Ruder, MS Linet, M Yeager, Z Wang, N Orr, HA Fine, D Kwon, G Thomas, N Rothman, PD Inskip, SJ Chanock
Publication Date: 2009-05

Variant appearance in text: rs308439
PubMed Link: 19423540
PubMed Central Link
Variant Present in the following documents:
  • NIHMS117439-supplement-Table_1.pdf
View BVdb publication page


Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000264498.3 c.578-23897T>G - intron_variant - 1/2
ENST00000608478.1 c.179-23897T>G - intron_variant - 1/2
NM_001361665.2 c.179-23897T>G - intron_variant - 1/2
NM_002006.5 c.578-23897T>G - intron_variant - 1/2