FLT4 c.1258+6_1258+10del

Variant ID: 5-180053100-CCCTGA-C

NM_182925.4(FLT4):c.1258+6_1258+10del

This variant was identified in 1 publication

View GRCh38 version.




Publications:


FLT4 Mutations Are Associated with Segmental Lymphatic Dysfunction and Initial Lymphatic Aplasia in Patients with Milroy Disease.

Genes
Liu, Ningfei N; Gao, Minzhe M
Publication Date: 2021-10-13

Variant appearance in text: FLT4: 1258+6_1258+10del
PubMed Link: 34681005
Variant Present in the following documents:
  • Main text
  • genes-12-01611.pdf
View BVdb publication page