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F2 c.532_534delinsCAT ;(p.R178H)
Variant ID: 11-46745041-AGG-CAT
NM_000506.3(
F2
):c.532_534delinsCAT;(p.R178H)
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:
A single amino acid substitution in IIIf subfamily of basic helix-loop-helix transcription factor AtMYC1 leads to trichome and root hair patterning defects by abolishing its interaction with partner proteins in Arabidopsis.
The Journal Of Biological Chemistry
Zhao, Hongtao H; Wang, Xiaoxue X; Zhu, Dandan D; Cui, Sujuan S; Li, Xia X; Cao, Ying Y; Ma, Ligeng L
Publication Date: 2012-04-20
Variant appearance in text: F2: R178H
PubMed Link:
22334670
Variant Present in the following documents:
Main text
View BVdb publication page