NOTCH1 c.4758_4759insCA ;(p.N1587Qfs*30)

Variant ID: 9-139399384-T-TTG

NM_017617.3(NOTCH1):c.4758_4759insCA;(p.N1587Qfs*30)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Disease-associated mosaic variation in clinical exome sequencing: a two-year pediatric tertiary care experience.

Cold Spring Harbor Molecular Case Studies
Miller, Cecelia R CR; Lee, Kristy K; Pfau, Ruthann B RB; Reshmi, Shalini C SC; Corsmeier, Donald J DJ; Hashimoto, Sayaka S; Dave-Wala, Ashita A; Jayaraman, Vijayakumar V; Koboldt, Daniel D; Matthews, Theodora T; Mouhlas, Danielle D; Stein, Maggie M; McKinney, Aimee A; Grossman, Tom T; Kelly, Benjamin J BJ; White, Peter P; Magrini, Vincent V; Wilson, Richard K RK; Mardis, Elaine R ER; Cottrell, Catherine E CE
Publication Date: 2020-06

Variant appearance in text: NOTCH1: 4758_4759insCA
PubMed Link: 32371413
Variant Present in the following documents:
  • Main text
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