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NSF c.697_698delinsGC ;(p.R233A)
Variant ID: 17-44720577-CG-GC
NM_006178.3(
NSF
):c.697_698delinsGC;(p.R233A)
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:
Systematic dissection and trajectory-scanning mutagenesis of the molecular interface that ensures specificity of two-component signaling pathways.
Plos Genetics
Capra, Emily J EJ; Perchuk, Barrett S BS; Lubin, Emma A EA; Ashenberg, Orr O; Skerker, Jeffrey M JM; Laub, Michael T MT
Publication Date: 2010-11-24
Variant appearance in text: NSF: R233A
PubMed Link:
21124821
Variant Present in the following documents:
Main text
pgen.1001220.pdf
View BVdb publication page