SI c.3308_3309delinsAT ;(p.S1103Y)

Variant ID: 3-164737504-CG-AT

NM_001041.3(SI):c.3308_3309delinsAT;(p.S1103Y)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Retrospective Genetic Analysis of 200 Cases of Sudden Infant Death Syndrome and Its Relationship with Long QT Syndrome in Korea.

Journal Of Korean Medical Science
Son, Min-Jeong MJ; Kim, Min-Kyoung MK; Yang, Kyung-Moo KM; Choi, Byung-Ha BH; Lee, Bong Woo BW; Yoo, Seong Ho SH
Publication Date: 2018-08-06

Variant appearance in text: SI: S1103Y
PubMed Link: 30079003
Variant Present in the following documents:
  • jkms-33-e200.pdf
View BVdb publication page