GRIN2A c.170C>T ;(p.P57L)

Variant ID: 16-10274099-G-A

NM_001134407.1(GRIN2A):c.170C>T;(p.P57L)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


GESPA: classifying nsSNPs to predict disease association.

Bmc Bioinformatics
Khurana, Jay K JK; Reeder, Jay E JE; Shrimpton, Antony E AE; Thakar, Juilee J
Publication Date: 2015-07-25

Variant appearance in text: GRIN2A: P57L
PubMed Link: 26206375
Variant Present in the following documents:
  • 12859_2015_673_MOESM1_ESM.xls, sheet 4
View BVdb publication page