PROK2 c.306G>C ;(p.R102S)

Variant ID: 3-71821959-C-G

NM_001126128.1(PROK2):c.306G>C;(p.R102S)

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:

Clinical, hormonal, and genetic characteristics of 25 Chinese patients with idiopathic hypogonadotropic hypogonadism.

Bmc Endocrine Disorders
Liu, Qingxu Q; Yin, Xiaoqin X; Li, Pin P
Publication Date: 2022-01-28

Variant appearance in text: PROK2: 306G>C; Arg102Ser
PubMed Link: 35090434
Variant Present in the following documents:
  • Main text
  • 12902_2022_Article_940.pdf
View BVdb publication page


Clinical, hormonal, and genetic characteristics of 25 Chinese patients with idiopathic hypogonadotropic hypogonadism.

Bmc Endocrine Disorders
Liu, Qingxu Q; Yin, Xiaoqin X; Li, Pin P
Publication Date: 2022-01-28

Variant appearance in text: PROK2: 306G>C; Arg102Ser
PubMed Link: 35090434
Variant Present in the following documents:
  • Main text
  • 12902_2022_Article_940.pdf
View BVdb publication page