SCN1A c.2779T>A ;(p.C927S)

Variant ID: 2-166894453-A-T

NM_001165963.1(SCN1A):c.2779T>A;(p.C927S)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Deep sequencing as a probe of normal stem cell fate and preneoplasia in human epidermis.

Proceedings Of The National Academy Of Sciences Of The United States Of America
Simons, Benjamin D BD
Publication Date: 2016-01-05

Variant appearance in text: SCN1A: C927S
PubMed Link: 26699486
Variant Present in the following documents:
  • Main text
View BVdb publication page