PROK2 c.153G>C ;(p.W51C)

Variant ID: 3-71830687-C-G

NM_001126128.1(PROK2):c.153G>C;(p.W51C)

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:

Analysis of PLXNA1, NRP1, and NRP2 variants in a cohort of patients with isolated hypogonadotropic hypogonadism.

Molecular Genetics & Genomic Medicine
Men, Meichao M; Chen, Dan-Na DN; Li, Jia-Da JD; Wang, Xinying X; Zeng, Wang W; Jiang, Fang F; Zheng, Ruizhi R; Dai, Wenting W
Publication Date: 2021-11

Variant appearance in text: PROK2: 153G>C; W51C
PubMed Link: 34636164
Variant Present in the following documents:
  • MGG3-9-e1816.pdf
View BVdb publication page


Analysis of PLXNA1, NRP1, and NRP2 variants in a cohort of patients with isolated hypogonadotropic hypogonadism.

Molecular Genetics & Genomic Medicine
Men, Meichao M; Chen, Dan-Na DN; Li, Jia-Da JD; Wang, Xinying X; Zeng, Wang W; Jiang, Fang F; Zheng, Ruizhi R; Dai, Wenting W
Publication Date: 2021-11

Variant appearance in text: PROK2: 153G>C; W51C
PubMed Link: 34636164
Variant Present in the following documents:
  • MGG3-9-e1816.pdf
View BVdb publication page