RYR1 c.1391A>G ;(p.Q464R)

Variant ID: 19-38943605-A-G

NM_000540.2(RYR1):c.1391A>G;(p.Q464R)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


De novo mutations in NALCN cause a syndrome characterized by congenital contractures of the limbs and face, hypotonia, and developmental delay.

American Journal Of Human Genetics
Chong, Jessica X JX; McMillin, Margaret J MJ; Shively, Kathryn M KM; Beck, Anita E AE; Marvin, Colby T CT; Armenteros, Jose R JR; Buckingham, Kati J KJ; Nkinsi, Naomi T NT; Boyle, Evan A EA; Berry, Margaret N MN; Bocian, Maureen M; Foulds, Nicola N; Uzielli, Maria Luisa Giovannucci ML; Haldeman-Englert, Chad C; Hennekam, Raoul C M RC; Kaplan, Paige P; Kline, Antonie D AD; Mercer, Catherine L CL; Nowaczyk, Malgorzata J M MJ; Klein Wassink-Ruiter, Jolien S JS; McPherson, Elizabeth W EW; Moreno, Regina A RA; Scheuerle, Angela E AE; Shashi, Vandana V; Stevens, Cathy A CA; Carey, John C JC; Monteil, Arnaud A; Lory, Philippe P; Tabor, Holly K HK; Smith, Joshua D JD; Shendure, Jay J; Nickerson, Deborah A DA; , ; Bamshad, Michael J MJ
Publication Date: 2015-03-05

Variant appearance in text: RYR1: 1391A>G; Gln464Arg
PubMed Link: 25683120
Variant Present in the following documents:
  • Main text
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