Bibliome.ai browser hg19
Search
About
Stats
FAQ
RUNX2 c.-120T>C
Variant ID: 6-45296144-T-C
NM_001024630.4(
RUNX2
):c.-120T>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:
Multi-layered mutation in hedgehog-related genes in Gorlin syndrome may affect the phenotype.
Plos One
Onodera, Shoko S; Saito, Akiko A; Hasegawa, Daigo D; Morita, Nana N; Watanabe, Katsuhito K; Nomura, Takeshi T; Shibahara, Takahiko T; Ohba, Shinsuke S; Yamaguchi, Akira A; Azuma, Toshifumi T
Publication Date: 2017
Variant appearance in text: rs535015975
PubMed Link:
28915250
Variant Present in the following documents:
Main text
pone.0184702.pdf
View BVdb publication page