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CHRNB2 c.297T>C ;(p.F99=)
Variant ID: 1-154542775-T-C
NM_000748.2(
CHRNB2
):c.297T>C;(p.F99=)
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:
Proteome-wide Structural Analysis of PTM Hotspots Reveals Regulatory Elements Predicted to Impact Biological Function and Disease.
Molecular & Cellular Proteomics : Mcp
Torres, Matthew P MP; Dewhurst, Henry H; Sundararaman, Niveda N
Publication Date: 2016-11
Variant appearance in text: CHRNB2: 297T>C; Phe99=
PubMed Link:
27697855
Variant Present in the following documents:
10.1074_M116.062331_mcp.M116.062331-3.xlsx, sheet 5
View BVdb publication page