基因突变(Mutation，在生物学上的含义，是指细胞中的遗传基因(通常指存在于细胞核中的去氧核糖核酸)发生的突然及永久性改变。它包括单个碱基改变所引起的点突变，或多个碱基的缺失、重复和插入。突变通常会导致细胞运作不正常、或细胞死亡，甚至可以在较高等生物中引发癌症。 304am永利集团推出 Mutation 标准品，适用于日常质控和性能验证，确保检测结果的高特异性和重复性，提高检测准确性。
BRAF p.G464E Reference Standard
CBP10697BRAF p.V600E Reference Standard
CBP10234BRAF p.N581Y Reference Standard
CBP10238BRAF p.L597V Reference Standard
CBP10241BRAF p.L597R Reference Standard
CBP10240BRAF p.K601N Reference Standard
CBP10237BRAF p.G596R Reference Standard
CBP10242BRAF p.G469R Reference Standard
CBP10236BRAF p.G469A Reference Standard
CBP10235BRAF p.G466V Reference Standard
CBP10239BRAF p.G464V Reference Standard
CBP10695AI-Edigene® BRAF p.V600R Reference Standard Plus
CBP10426AI-Edigene® BRAF p.V600M Reference Standard Plus
CBP10425AI-Edigene® BRAF p.V600K Reference Standard Plus
CBP10413AI-Edigene® BRAF p.V600G Reference Standard Plus
CBP10427AI-Edigene® BRAF p.V600E Reference Standard Plus
CBP10424AI-Edigene® BRAF p.V600D Reference Standard Plus
CBP10423AI-Edigene® BRAF p.K601E Reference Standard Plus
CBP10428BRCA1 p.L392_Q405del Reference Standard
CBP10705BRCA1 Splice Donor Site Mutation (c.5390+1G>A) Reference Standard
CBP10432BRCA1 p.W1815C Reference Standard
CBP10346BRCA1 p.V1809fs*20 Reference Standard
CBP10361BRCA1 p.S663N Reference Standard
CBP10359BRCA1 p.S114T Reference Standard
CBP10356BRCA1 p.R1751* Reference Standard
CBP10358BRCA1 p.Q1756fs Reference Standard
CBP10360BRCA1 p.P724fs*12 Reference Standard
CBP10364BRCA1 p.P1190H Reference Standard
CBP10349BRCA1 p.N976S Reference Standard
CBP10351BRCA1 p.N810T Reference Standard
CBP10353BRCA1 p.N742S Reference Standard
CBP10354BRCA1 p.M1014I Reference Standard
CBP10348BRCA1 p.K654fs*47 Reference Standard
CBP10362BRCA1 p.I456T Reference Standard
CBP10357BRCA1 p.I1058V Reference Standard
CBP10355BRCA1 p.G401E Reference Standard
CBP10350BRCA1 p.E962K Reference Standard
CBP10352BRCA1 p.E23fs*17 Reference Standard
CBP10363BRCA1 p.D435Y Reference Standard
CBP10347BRCA2 Splice Donor Site Mutation (c.1909+2T>C) Reference Standard
CBP10466BRCA2 p.V1862fs*1 Reference Standard
CBP10385BRCA2 p.V1810I Reference Standard
CBP10367BRCA2 p.T3085fs*26 Reference Standard
CBP10400BRCA2 p.T3033fs*29 Reference Standard
CBP10398BRCA2 p.T3033fs*11 Reference Standard
CBP10399BRCA2 p.T3033fs*11 Reference Standard
CBP10380BRCA2 p.S3094* Reference Standard
CBP10375BRCA2 p.S2284L Reference Standard
CBP10370BRCA2 p.S1982fs*22 Reference Standard
CBP10389BRCA2 p.S1461fs*2 Reference Standard
CBP10379BRCA2 p.R2973C Reference Standard
CBP10374BRCA2 p.R2318* Reference Standard
CBP10376BRCA2 p.R2287fs*4 Reference Standard
CBP10395BRCA2 p.Q2934* Reference Standard
CBP10397BRCA2 p.Q1782fs Reference Standard
CBP10460BRCA2 p.Q1429fs*9 Reference Standard
CBP10387BRCA2 p.N986fs*5 Reference Standard
CBP10378BRCA2 p.N856Y Reference Standard
CBP10368BRCA2 p.N1822fs*2 Reference Standard
CBP10388BRCA2 p.N1784fs*7 Reference Standard
CBP10390BRCA2 p.N1784fs*3 Reference Standard
CBP10391BRCA2 p.N1287fs*6 Reference Standard
CBP10393BRCA2 p.N1100T Reference Standard
CBP10384BRCA2 p.K1691Nfs*15 Reference Standard
CBP10547BRCA2 p.K1517fs*23 Reference Standard
CBP10377BRCA2 p.K1487K Reference Standard
CBP10382BRCA2 p.I2675fs*6 Reference Standard
CBP10396BRCA2 p.G1376E Reference Standard
CBP10373BRCA2 p.F1524F Reference Standard
CBP10383BRCA2 p.F1427fs Reference Standard
CBP10454BRCA2 p.E2981fs*37 Reference Standard
CBP10381BRCA2 p.E2292A Reference Standard
CBP10566BRCA2 p.E1593* Reference Standard
CBP10366BRCA2 p.E1518Q Reference Standard
CBP10369BRCA2 p.D1476G Reference Standard
CBP10371BRCA2 p.C1200fs*1 Reference Standard
CBP10386BRCA2 p.A487V Reference Standard
CBP10372BRCA2 p.A3029T Reference Standard
CBP10365BRCA2 Insertion (216bp)
CBP10552BRCA2 Deletion (2135bp del)
CBP10505BRCA2 Deletion (1419bp del)
CBP10506
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