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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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