TAS2R31 c.820A>G ;(p.I274V)

Variant ID: 12-11183115-T-C

NM_176885.2(TAS2R31):c.820A>G;(p.I274V)

This variant was identified in 9 publications

View GRCh38 version.




Publications:


Genetic analysis of sinonasal undifferentiated carcinoma discovers recurrent SWI/SNF alterations and a novel PGAP3-SRPK1 fusion gene.

Bmc Cancer
Heft Neal, Molly E ME; Birkeland, Andrew C AC; Bhangale, Apurva D AD; Zhai, Jingyi J; Kulkarni, Aditi A; Foltin, Susan K SK; Jewell, Brittany M BM; Ludwig, Megan L ML; Pinatti, Lisa L; Jiang, Hui H; McHugh, Jonathan B JB; Marentette, Lawence L; McKean, Erin L EL; Brenner, J Chad JC
Publication Date: 2021-05-29

Variant appearance in text: rs770006497
PubMed Link: 34051734
Variant Present in the following documents:
  • 12885_2021_8370_MOESM15_ESM.xlsx, sheet 1
View BVdb publication page



Disseminated Talaromyces marneffei Infection in a Non-HIV Infant With a Homozygous Private Variant of RELB.

Frontiers In Cellular And Infection Microbiology
Ding, Xiaofang X; Huang, Han H; Zhong, Lili L; Chen, Min M; Peng, Fang F; Zhang, Bing B; Cui, Xinyu X; Yang, Xiu-An XA
Publication Date: 2021

Variant appearance in text: TAS2R31: I274V; rs770006497
PubMed Link: 33791233
Variant Present in the following documents:
  • Table_2.xlsx, sheet 1
View BVdb publication page



Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani families.

Bmc Medical Genetics
Zhou, Yingjie Y; Tariq, Muhammad M; He, Sijie S; Abdullah, Uzma U; Zhang, Jianguo J; Baig, Shahid Mahmood SM
Publication Date: 2020-07-18

Variant appearance in text: TAS2R31: 820A>G; Ile274Val
PubMed Link: 32682410
Variant Present in the following documents:
  • 12881_2020_1087_MOESM1_ESM.xlsx, sheet 4
  • 12881_2020_1087_MOESM1_ESM.xlsx, sheet 6
  • 12881_2020_1087_MOESM1_ESM.xlsx, sheet 5
  • 12881_2020_1087_MOESM1_ESM.xlsx, sheet 3
View BVdb publication page



A Bitter Taste in Your Heart.

Frontiers In Physiology
Bloxham, Conor J CJ; Foster, Simon R SR; Thomas, Walter G WG
Publication Date: 2020

Variant appearance in text: T2R31: I274V
PubMed Link: 32457649
Variant Present in the following documents:
  • Main text
  • fphys-11-00431.pdf
View BVdb publication page



Novel NOG (p.P42S) mutation causes proximal symphalangism in a four-generation Chinese family.

Bmc Medical Genetics
Sha, Yanwei Y; Ma, Ding D; Zhang, Ning N; Wei, Xiaoli X; Liu, Wensheng W; Wang, Xiong X
Publication Date: 2019-08-01

Variant appearance in text: TAS2R31: I274V; rs770006497
PubMed Link: 31370824
Variant Present in the following documents:
  • 12881_2019_864_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Synthetic modeling reveals HOXB genes are critical for the initiation and maintenance of human leukemia.

Nature Communications
Kusakabe, Manabu M; Sun, Ann Chong AC; Tyshchenko, Kateryna K; Wong, Rachel R; Nanda, Aastha A; Shanna, Claire C; Gusscott, Samuel S; Chavez, Elizabeth A EA; Lorzadeh, Alireza A; Zhu, Alice A; Hill, Ainsleigh A; Hung, Stacy S; Brown, Scott S; Babaian, Artem A; Wang, Xuehai X; Holt, Robert A RA; Steidl, Christian C; Karsan, Aly A; Humphries, R Keith RK; Eaves, Connie J CJ; Hirst, Martin M; Weng, Andrew P AP
Publication Date: 2019-07-02

Variant appearance in text: TAS2R31: 820A>G; Ile274Val
PubMed Link: 31266935
Variant Present in the following documents:
  • 41467_2019_10510_MOESM8_ESM.xlsx, sheet 1
  • 41467_2019_10510_MOESM8_ESM.xlsx, sheet 2
View BVdb publication page



Genomic case report of a low grade bladder tumor metastasis to lung.

Bmc Urology
Van Every, Marvin J MJ; Dancik, Garrett G; Paramesh, Venki V; Gurda, Grzegorz T GT; Meier, David R DR; Cash, Steven E SE; Richmond, Craig S CS; Guin, Sunny S
Publication Date: 2018-09-03

Variant appearance in text: TAS2R31: 820A>G; Ile274Val
PubMed Link: 30176882
Variant Present in the following documents:
  • 12894_2018_386_MOESM5_ESM.xlsx, sheet 5
View BVdb publication page



Renal hypouricemia caused by novel compound heterozygous mutations in the SLC22A12 gene: a case report with literature review.

Bmc Medical Genetics
Zhou, Zhaowei Z; Ma, Lidan L; Zhou, Juan J; Song, Zhijian Z; Zhang, Jinmai J; Wang, Ke K; Chen, Boyu B; Pan, Dun D; Li, Zhiqiang Z; Li, Changgui C; Shi, Yongyong Y
Publication Date: 2018-08-10

Variant appearance in text: TAS2R31: I274V
PubMed Link: 30097038
Variant Present in the following documents:
  • 12881_2018_595_MOESM1_ESM.xlsx, sheet 2
View BVdb publication page



Co-existence of BRAF and NRAS driver mutations in the same melanoma cells results in heterogeneity of targeted therapy resistance.

Oncotarget
Raaijmakers, Marieke I G MI; Widmer, Daniel S DS; Narechania, Apurva A; Eichhoff, Ossia O; Freiberger, Sandra N SN; Wenzina, Judith J; Cheng, Phil F PF; Mihic-Probst, Daniela D; Desalle, Rob R; Dummer, Reinhard R; Levesque, Mitchell P MP
Publication Date: 2016-11-22

Variant appearance in text: TAS2R31: I274V
PubMed Link: 27791198
Variant Present in the following documents:
  • oncotarget-07-77163-s003.xlsx, sheet 1
  • oncotarget-07-77163-s003.xlsx, sheet 8
  • oncotarget-07-77163-s002.xlsx, sheet 8
  • oncotarget-07-77163-s003.xlsx, sheet 4
  • oncotarget-07-77163-s002.xlsx, sheet 4
  • oncotarget-07-77163-s002.xlsx, sheet 3
  • oncotarget-07-77163-s002.xlsx, sheet 1
  • oncotarget-07-77163-s003.xlsx, sheet 3
View BVdb publication page