Bibliome.ai browser hg19
Search
About
Stats
FAQ
KCNH5 c.1730T>G ;(p.I577S)
Variant ID: 14-63269139-A-C
NM_139318.4(
KCNH5
):c.1730T>G;(p.I577S)
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:
Identification of biomarkers complementary to homologous recombination deficiency for improving the clinical outcome of ovarian serous cystadenocarcinoma.
Clinical And Translational Medicine
Shi, Zhiwen Z; Zhao, Qingguo Q; Lv, Bin B; Qu, Xinyu X; Han, Xiao X; Wang, Hongyan H; Qiu, Junjun J; Hua, Keqin K
Publication Date: 2021-05
Variant appearance in text: KCNH5: 1730T>G; I577S
PubMed Link:
34047476
Variant Present in the following documents:
CTM2-11-e399-s003.xls, sheet 1
View BVdb publication page