SCN1A c.4282G>A ;(p.V1428I)

Variant ID: 2-166858984-C-T

NM_001165963.1(SCN1A):c.4282G>A;(p.V1428I)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Calibration of computational tools for missense variant pathogenicity classification and ClinGen recommendations for PP3/BP4 criteria.

American Journal Of Human Genetics
Pejaver, Vikas V; Byrne, Alicia B AB; Feng, Bing-Jian BJ; Pagel, Kymberleigh A KA; Mooney, Sean D SD; Karchin, Rachel R; O'Donnell-Luria, Anne A; Harrison, Steven M SM; Tavtigian, Sean V SV; Greenblatt, Marc S MS; Biesecker, Leslie G LG; Radivojac, Predrag P; Brenner, Steven E SE; ,
Publication Date: 2022-12-01

Variant appearance in text: SCN1A: V1428I
PubMed Link: 36413997
Variant Present in the following documents:
  • mmc2.xlsx, sheet 1
View BVdb publication page



Genomic analysis of 21 patients with corneal neuralgia after refractive surgery.

Pain Reports
Yuan, Jun-Hui JH; Schulman, Betsy R BR; Effraim, Philip R PR; Sulayman, Dib-Hajj DH; Jacobs, Deborah S DS; Waxman, Stephen G SG
Publication Date: 2020

Variant appearance in text: SCN1A: V1428I
PubMed Link: 32766464
Variant Present in the following documents:
  • Main text
  • painreports-5-e826.pdf
View BVdb publication page