SCN1A c.4736T>C ;(p.V1579A)

Variant ID: 2-166850772-A-G

NM_001165963.1(SCN1A):c.4736T>C;(p.V1579A)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Whole-genome analysis for effective clinical diagnosis and gene discovery in early infantile epileptic encephalopathy.

Npj Genomic Medicine
Ostrander, Betsy E P BEP; Butterfield, Russell J RJ; Pedersen, Brent S BS; Farrell, Andrew J AJ; Layer, Ryan M RM; Ward, Alistair A; Miller, Chase C; DiSera, Tonya T; Filloux, Francis M FM; Candee, Meghan S MS; Newcomb, Tara T; Bonkowsky, Joshua L JL; Marth, Gabor T GT; Quinlan, Aaron R AR
Publication Date: 2018

Variant appearance in text: SCN1A: 4736T>C
PubMed Link: 30109124
Variant Present in the following documents:
  • Main text
  • 41525_2018_61_MOESM1_ESM.xlsx, sheet 5
View BVdb publication page