RET c.868-409G>C

Variant ID: 10-43601415-G-C

NM_020975.4(RET):c.868-409G>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Familial multinodular goiter syndrome with papillary thyroid carcinomas: mutational analysis of the associated genes in 5 cases from 1 Chinese family.

Bmc Endocrine Disorders
Liao, Shunyao S; Song, Wenzhong W; Liu, Yunqiang Y; Deng, Shaoping S; Liang, Yaming Y; Tang, Zhenlin Z; Huang, Jiyuan J; Dong, Dandan D; Xu, Gang G
Publication Date: 2013-10-21

Variant appearance in text: rs35800403
PubMed Link: 24144365
Variant Present in the following documents:
  • Main text
  • 1472-6823-13-48.pdf
View BVdb publication page