ACSM5 c.370C>A ;(p.R124=)

Variant ID: 16-20429546-C-A

NM_017888.2(ACSM5):c.370C>A;(p.R124=)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome.

G3 (Bethesda, Md.)
Merico, Daniele D; Zarrei, Mehdi M; Costain, Gregory G; Ogura, Lucas L; Alipanahi, Babak B; Gazzellone, Matthew J MJ; Butcher, Nancy J NJ; Thiruvahindrapuram, Bhooma B; Nalpathamkalam, Thomas T; Chow, Eva W C EW; Andrade, Danielle M DM; Frey, Brendan J BJ; Marshall, Christian R CR; Scherer, Stephen W SW; Bassett, Anne S AS
Publication Date: 2015-09-16

Variant appearance in text: rs144548629
PubMed Link: 26384369
Variant Present in the following documents:
  • supp_g3.115.021345_TableS1.xlsx, sheet 1
View BVdb publication page