OAS1 c.180+232C>G

Variant ID: 12-113345256-C-G

NM_016816.2(OAS1):c.180+232C>G

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem
Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS
Publication Date: 2022-11

Variant appearance in text: rs10744785
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: OAS1: 180+232C>G; rs10744785
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_5.xlsx, sheet 1
View BVdb publication page



Genetic polymorphisms in host antiviral genes: associations with humoral and cellular immunity to measles vaccine.

Vaccine
Haralambieva, Iana H IH; Ovsyannikova, Inna G IG; Umlauf, Benjamin J BJ; Vierkant, Robert A RA; Shane Pankratz, V V; Jacobson, Robert M RM; Poland, Gregory A GA
Publication Date: 2011-11-08

Variant appearance in text: rs10744785
PubMed Link: 21939710
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page



Genetic variation in OAS1 is a risk factor for initial infection with West Nile virus in man.

Plos Pathogens
Lim, Jean K JK; Lisco, Andrea A; McDermott, David H DH; Huynh, Linda L; Ward, Jerrold M JM; Johnson, Bernard B; Johnson, Hope H; Pape, John J; Foster, Gregory A GA; Krysztof, David D; Follmann, Dean D; Stramer, Susan L SL; Margolis, Leonid B LB; Murphy, Philip M PM
Publication Date: 2009-02

Variant appearance in text: rs10744785
PubMed Link: 19247438
Variant Present in the following documents:
  • Main text
  • ppat.1000321.pdf
View BVdb publication page



Identification of common genetic variants that account for transcript isoform variation between human populations.

Human Genetics
Zhang, Wei W; Duan, Shiwei S; Bleibel, Wasim K WK; Wisel, Steven A SA; Huang, R Stephanie RS; Wu, Xiaolin X; He, Lijun L; Clark, Tyson A TA; Chen, Tina X TX; Schweitzer, Anthony C AC; Blume, John E JE; Dolan, M Eileen ME; Cox, Nancy J NJ
Publication Date: 2009-02

Variant appearance in text: rs10744785
PubMed Link: 19052777
Variant Present in the following documents:
  • Main text
View BVdb publication page