SI c.2159+2T>G

Variant ID: 3-164758726-A-C

NM_001041.3(SI):c.2159+2T>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Two Novel Mutations in the SI Gene Associated With Congenital Sucrase-Isomaltase Deficiency: A Case Report in China.

Frontiers In Pediatrics
Zhou, Jianli J; Zhao, Yuzhen Y; Qian, Xia X; Cheng, Yongwei Y; Cai, Huabo H; Chen, Moxian M; Zhou, Shaoming S
Publication Date: 2021

Variant appearance in text: SI: 2159+2T>G
PubMed Link: 34926337
Variant Present in the following documents:
  • Main text
  • fped-09-731716.pdf
View BVdb publication page