HP c.1139G>A ;(p.S380N)

Variant ID: 16-72094707-G-A

NM_005143.3(HP):c.1139G>A;(p.S380N)

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 and functional analysis of CORIN variants in hypertensive patients.

Human Mutation
Zhang, Yue Y; Zhou, Tiantian T; Niu, Yayan Y; He, Meiling M; Wang, Can C; Liu, Meng M; Yang, Junhua J; Zhang, Yonghong Y; Zhou, Jianping J; Fukuda, Koichi K; Qin, Jun J; Dong, Ningzheng N; Wu, Qingyu Q
Publication Date: 2017-12

Variant appearance in text: HP: 1139G>A
PubMed Link: 28861913
Variant Present in the following documents:
  • Main text
View BVdb publication page