EPHB2 c.1463G>C ;(p.S488T)

Variant ID: 1-23219411-G-C

NM_017449.3(EPHB2):c.1463G>C;(p.S488T)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Association of GBA Mutations and the E326K Polymorphism With Motor and Cognitive Progression in Parkinson Disease.

Jama Neurology
Davis, Marie Y MY; Johnson, Catherine O CO; Leverenz, James B JB; Weintraub, Daniel D; Trojanowski, John Q JQ; Chen-Plotkin, Alice A; Van Deerlin, Vivianna M VM; Quinn, Joseph F JF; Chung, Kathryn A KA; Peterson-Hiller, Amie L AL; Rosenthal, Liana S LS; Dawson, Ted M TM; Albert, Marilyn S MS; Goldman, Jennifer G JG; Stebbins, Glenn T GT; Bernard, Bryan B; Wszolek, Zbigniew K ZK; Ross, Owen A OA; Dickson, Dennis W DW; Eidelberg, David D; Mattis, Paul J PJ; Niethammer, Martin M; Yearout, Dora D; Hu, Shu-Ching SC; Cholerton, Brenna A BA; Smith, Megan M; Mata, Ignacio F IF; Montine, Thomas J TJ; Edwards, Karen L KL; Zabetian, Cyrus P CP
Publication Date: 2016-10-01

Variant appearance in text: DRT: S488T
PubMed Link: 27571329
Variant Present in the following documents:
  • Main text
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