Bibliome.ai browser hg19
Search
About
Stats
FAQ
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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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