KRAS c.450+2749G>T

Variant ID: 12-25375799-C-A

NM_004985.3(KRAS):c.450+2749G>T

This variant was identified in 4 publications

View GRCh38 version.




Publications:


Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs12579073
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



A pharmacogenomic approach to the treatment of children with GH deficiency or Turner syndrome.

European Journal Of Endocrinology
Clayton, P P; Chatelain, P P; Tatò, L L; Yoo, H W HW; Ambler, G R GR; Belgorosky, A A; Quinteiro, S S; Deal, C C; Stevens, A A; Raelson, J J; Croteau, P P; Destenaves, B B; Olivier, C C
Publication Date: 2013-09

Variant appearance in text: rs12579073
PubMed Link: 23761422
Variant Present in the following documents:
  • Main text
  • EJE130069.pdf
View BVdb publication page



Tagging single-nucleotide polymorphisms in candidate oncogenes and susceptibility to ovarian cancer.

British Journal Of Cancer
Quaye, L L; Song, H H; Ramus, S J SJ; Gentry-Maharaj, A A; Høgdall, E E; DiCioccio, R A RA; McGuire, V V; Wu, A H AH; Van Den Berg, D J DJ; Pike, M C MC; Wozniak, E E; Doherty, J A JA; Rossing, M A MA; Ness, R B RB; Moysich, K B KB; Høgdall, C C; Blaakaer, J J; , ; Easton, D F DF; Ponder, B A J BA; Jacobs, I J IJ; Menon, U U; Whittemore, A S AS; Krüger-Kjaer, S S; Pearce, C L CL; Pharoah, P D P PD; Gayther, S A SA
Publication Date: 2009-03-24

Variant appearance in text: rs12579073
PubMed Link: 19240718
Variant Present in the following documents:
  • Main text
  • 6604947a.pdf
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Functional genetic polymorphisms and female reproductive disorders: part II--endometriosis.

Human Reproduction Update
Tempfer, C B CB; Simoni, M M; Destenaves, B B; Fauser, B C J M BC
Publication Date: 2009

Variant appearance in text: rs12579073
PubMed Link: 18805939
Variant Present in the following documents:
  • Main text
View BVdb publication page