JAG1 c.1207C>T ;(p.Q403*)

Variant ID: 20-10630922-G-A

NM_000214.2(JAG1):c.1207C>T;(p.Q403*)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Alagille syndrome mutation update: Comprehensive overview of JAG1 and NOTCH2 mutation frequencies and insight into missense variant classification.

Human Mutation
Gilbert, Melissa A MA; Bauer, Robert C RC; Rajagopalan, Ramakrishnan R; Grochowski, Christopher M CM; Chao, Grace G; McEldrew, Deborah D; Nassur, James A JA; Rand, Elizabeth B EB; Krock, Bryan L BL; Kamath, Binita M BM; Krantz, Ian D ID; Piccoli, David A DA; Loomes, Kathleen M KM; Spinner, Nancy B NB
Publication Date: 2019-12

Variant appearance in text: JAG1: Gln403*
PubMed Link: 31343788
Variant Present in the following documents:
  • Main text
  • HUMU-40-2197.pdf
View BVdb publication page



Spectrum of JAG1 gene mutations in Polish patients with Alagille syndrome.

Journal Of Applied Genetics
Jurkiewicz, Dorota D; Gliwicz, Dorota D; Ciara, Elżbieta E; Gerfen, Jennifer J; Pelc, Magdalena M; Piekutowska-Abramczuk, Dorota D; Kugaudo, Monika M; Chrzanowska, Krystyna K; Spinner, Nancy B NB; Krajewska-Walasek, Małgorzata M
Publication Date: 2014-08

Variant appearance in text: JAG1: 1207C>T; Gln403Ter
PubMed Link: 24748328
Variant Present in the following documents:
  • Main text
  • 13353_2014_Article_212.pdf
View BVdb publication page