INTU c.1260-1001T>C

Variant ID: 4-128607832-T-C

NM_015693.3(INTU):c.1260-1001T>C

This variant was identified in 6 publications

View GRCh38 version.




Publications:


Machine learning based combination of multi-omics data for subgroup identification in non-small cell lung cancer.

Scientific Reports
Khadirnaikar, Seema S; Shukla, Sudhanshu S; Prasanna, S R M SRM
Publication Date: 2023-03-21

Variant appearance in text: rs2125573
PubMed Link: 36944673
Variant Present in the following documents:
  • 41598_2023_31426_MOESM3_ESM.xlsx, sheet 3
View BVdb publication page



Feasibility and ethics of using data from the Scottish newborn blood spot archive for research.

Communications Medicine
Cunningham-Burley, Sarah S; McCartney, Daniel L DL; Campbell, Archie A; Flaig, Robin R; Orange, Clare E L CEL; Porteous, Carol C; Aitken, Mhairi M; Mulholland, Ciaran C; Davidson, Sara S; McCafferty, Selena M SM; Murphy, Lee L; Wrobel, Nicola N; McCafferty, Sarah S; Wallace, Karen K; StClair, David D; Kerr, Shona S; Hayward, Caroline C; McIntosh, Andrew M AM; Sudlow, Cathie C; Marioni, Riccardo E RE; Pell, Jill J; Miedzybrodzka, Zosia Z; Porteous, David J DJ
Publication Date: 2022

Variant appearance in text: rs2125573
PubMed Link: 36210800
Variant Present in the following documents:
  • 43856_2022_189_MOESM1_ESM.pdf
View BVdb publication page



DNA methylation of chronic lymphocytic leukemia with differential response to chemotherapy.

Scientific Data
Yosifov, Deyan Yordanov DY; Bloehdorn, Johannes J; Döhner, Hartmut H; Lichter, Peter P; Stilgenbauer, Stephan S; Mertens, Daniel D
Publication Date: 2020-05-01

Variant appearance in text: rs2125573
PubMed Link: 32358561
Variant Present in the following documents:
  • 41597_2020_Article_456.pdf
View BVdb publication page



Intraventricular meningiomas frequently harbor NF2 mutations but lack common genetic alterations in TRAF7, AKT1, SMO, KLF4, PIK3CA, and TERT.

Acta Neuropathologica Communications
Jungwirth, Gerhard G; Warta, Rolf R; Beynon, Christopher C; Sahm, Felix F; von Deimling, Andreas A; Unterberg, Andreas A; Herold-Mende, Christel C; Jungk, Christine C
Publication Date: 2019-08-30

Variant appearance in text: rs2125573
PubMed Link: 31470906
Variant Present in the following documents:
  • 40478_2019_793_MOESM1_ESM.xlsx, sheet 2
View BVdb publication page



Identification of EML4-ALK as an alternative fusion gene in epithelioid inflammatory myofibroblastic sarcoma.

Orphanet Journal Of Rare Diseases
Jiang, Quan Q; Tong, Han-Xing HX; Hou, Ying-Yong YY; Zhang, Yong Y; Li, Jing-Lei JL; Zhou, Yu-Hong YH; Xu, Jing J; Wang, Jiong-Yuan JY; Lu, Wei-Qi WQ
Publication Date: 2017-05-23

Variant appearance in text: rs2125573
PubMed Link: 28535796
Variant Present in the following documents:
  • 13023_2017_647_MOESM1_ESM.xlsx, sheet 4
View BVdb publication page



Integrated transcriptome and methylome analysis in youth at high risk for bipolar disorder: a preliminary analysis.

Translational Psychiatry
Fries, G R GR; Quevedo, J J; Zeni, C P CP; Kazimi, I F IF; Zunta-Soares, G G; Spiker, D E DE; Bowden, C L CL; Walss-Bass, C C; Soares, J C JC
Publication Date: 2017-03-14

Variant appearance in text: rs2125573
PubMed Link: 28291257
Variant Present in the following documents:
  • tp201732x1.pdf
View BVdb publication page