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SI c.394_396delinsTGT ;(p.R132C)
Variant ID: 3-164786597-CCT-ACA
NM_001041.3(
SI
):c.394_396delinsTGT;(p.R132C)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Toward Single-Organelle Lipidomics in Live Cells.
Analytical Chemistry
Lita, Adrian A; Kuzmin, Andrey N AN; Pliss, Artem A; Baev, Alexander A; Rzhevskii, Alexander A; Gilbert, Mark R MR; Larion, Mioara M; Prasad, Paras N PN
Publication Date: 2019-09-03
Variant appearance in text: SI: R132C
PubMed Link:
31381322
Variant Present in the following documents:
Main text
View BVdb publication page
Clonal evolution revealed by whole genome sequencing in a case of primary myelofibrosis transformed to secondary acute myeloid leukemia.
Leukemia
Engle, E K EK; Fisher, D A C DA; Miller, C A CA; McLellan, M D MD; Fulton, R S RS; Moore, D M DM; Wilson, R K RK; Ley, T J TJ; Oh, S T ST
Publication Date: 2015-04
Variant appearance in text: SI: R132C
PubMed Link:
25252869
Variant Present in the following documents:
nihms629795.pdf
View BVdb publication page