EGF c.1526del ;(p.Q509Rfs*9)

Variant ID: 4-110885644-CA-C

NM_001963.4(EGF):c.1526del;(p.Q509Rfs*9)

This variant was identified in 1 publication

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: EGF: 1526del
PubMed Link: 31343788
Variant Present in the following documents:
  • Main text
  • HUMU-40-2197.pdf
View BVdb publication page