ASAH1 c.*926A>G

Variant ID: 8-17914117-T-C

NM_177924.3(ASAH1):c.*926A>G

This variant was identified in 9 publications

View GRCh38 version.




Publications:


Genome-wide association mapping and genomic prediction of agronomical traits and breeding values in Iranian wheat under rain-fed and well-watered conditions.

Bmc Genomics
Rabieyan, Ehsan E; Bihamta, Mohammad Reza MR; Moghaddam, Mohsen Esmaeilzadeh ME; Mohammadi, Valiollah V; Alipour, Hadi H
Publication Date: 2022-12-15

Variant appearance in text: rs3810
PubMed Link: 36522726
Variant Present in the following documents:
  • Main text
  • 12864_2022_Article_8968.pdf
View BVdb publication page



Beneficial effects of mifepristone treatment in breast cancer patients selected by the progesterone receptor isoform ratio: Results from the MIPRA trial.

Clinical Cancer Research : An Official Journal Of The American Association For Cancer Research
Elía, Andrés A; Saldain, Leo L; Vanzulli, Silvia I SI; Helguero, Luisa A LA; Lamb, Caroline A CA; Fabris, Victoria V; Pataccini, Gabriela G; Martínez-Vazquez, Paula P; Burruchaga, Javier J; Caillet-Bois, Ines I; Spengler, Eunice E; Acosta Haab, Gabriela G; Liguori, Marcos M; Castets, Alejandra A; Lovisi, Silvia S; Abascal, María F MF; Novaro, Virginia V; Sánchez, Jana J; Muñoz, Javier J; Belizán, Jose M JM; Abba, Martín C MC; Gass, Hugo H; Rojas, Paola P; Lanari, Claudia C
Publication Date: 2022-10-21

Variant appearance in text: rs3810
PubMed Link: 36269797
Variant Present in the following documents:
  • ccr-22-2060_supplementary_table_s5_suppts5.xlsx, sheet 1
View BVdb publication page



Next-generation sequencing identified novel Desmoplakin frame-shift variant in patients with Arrhythmogenic cardiomyopathy.

Bmc Cardiovascular Disorders
Lin, Xiaoping X; Ma, Yuankun Y; Cai, Zhejun Z; Wang, Qiyuan Q; Wang, Lihua L; Huo, Zhaoxia Z; Hu, Dan D; Wang, Jian'an J; Xiang, Meixiang M
Publication Date: 2020-02-11

Variant appearance in text: rs3810
PubMed Link: 32046637
Variant Present in the following documents:
  • 12872_2020_1369_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page



PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations.

Genome Biology
Zhang, Chao C; Gao, Yang Y; Ning, Zhilin Z; Lu, Yan Y; Zhang, Xiaoxi X; Liu, Jiaojiao J; Xie, Bo B; Xue, Zhe Z; Wang, Xiaoji X; Yuan, Kai K; Ge, Xueling X; Pan, Yuwen Y; Liu, Chang C; Tian, Lei L; Wang, Yuchen Y; Lu, Dongsheng D; Hoh, Boon-Peng BP; Xu, Shuhua S
Publication Date: 2019-10-22

Variant appearance in text: rs3810
PubMed Link: 31640808
Variant Present in the following documents:
  • 13059_2019_1838_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



Genetic Variation in Acid Ceramidase Predicts Non-completion of an Exercise Intervention.

Frontiers In Physiology
Lewis, Lauren S LS; Huffman, Kim M KM; Smith, Ira J IJ; Donahue, Mark P MP; Slentz, Cris A CA; Houmard, Joseph A JA; Hubal, Monica J MJ; Hoffman, Eric P EP; Hauser, Elizabeth R ER; Siegler, Ilene C IC; Kraus, William E WE
Publication Date: 2018

Variant appearance in text: rs3810
PubMed Link: 30008672
Variant Present in the following documents:
  • Main text
  • fphys-09-00781.pdf
View BVdb publication page



Genetic Control of Left Atrial Gene Expression Yields Insights into the Genetic Susceptibility for Atrial Fibrillation.

Circulation. Genomic And Precision Medicine
Hsu, Jeffrey J; Gore-Panter, Shamone S; Tchou, Gregory G; Castel, Laurie L; Lovano, Beth B; Moravec, Christine S CS; Pettersson, Gosta B GB; Roselli, Eric E EE; Gillinov, A Marc AM; McCurry, Kenneth R KR; Smedira, Nicholas G NG; Barnard, John J; Van Wagoner, David R DR; Chung, Mina K MK; Smith, Jonathan D JD
Publication Date: 2018-03

Variant appearance in text: rs3810
PubMed Link: 29545482
Variant Present in the following documents:
  • Main text
View BVdb publication page



Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.

Oncotarget
Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH
Publication Date: 2017-11-10

Variant appearance in text: rs3810
PubMed Link: 29221171
Variant Present in the following documents:
  • oncotarget-08-95841-s002.xlsx, sheet 1
  • oncotarget-08-95841-s002.xlsx, sheet 4
View BVdb publication page



Proteogenomic analysis reveals exosomes are more oncogenic than ectosomes.

Oncotarget
Keerthikumar, Shivakumar S; Gangoda, Lahiru L; Liem, Michael M; Fonseka, Pamali P; Atukorala, Ishara I; Ozcitti, Cemil C; Mechler, Adam A; Adda, Christopher G CG; Ang, Ching-Seng CS; Mathivanan, Suresh S
Publication Date: 2015-06-20

Variant appearance in text: rs3810
PubMed Link: 25944692
Variant Present in the following documents:
  • oncotarget-06-15375-s005.xlsx, sheet 2
View BVdb publication page



Powerful SNP-set analysis for case-control genome-wide association studies.

American Journal Of Human Genetics
Wu, Michael C MC; Kraft, Peter P; Epstein, Michael P MP; Taylor, Deanne M DM; Chanock, Stephen J SJ; Hunter, David J DJ; Lin, Xihong X
Publication Date: 2010-06-11

Variant appearance in text: rs3810
PubMed Link: 20560208
Variant Present in the following documents:
  • Main text
View BVdb publication page