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Nucleotide Change | Amino Acid Change | Mutation Frequency |
c.2573T>G | p.L858R | 0.0976 |
c.2235_2249del15 | p.E746_A750del | 0.0423 |
c.2236_2250del15 | p.E746_A750del | 0.0236 |
c.2240_2257del18 | p.L747_P753>S | 0.0088 |
c.2369C>T | p.T790M | 0.0061 |
c.2239_2248TTAAGAGAAG>C | p.L747_A750>P | 0.0057 |
c.2237_2255>T | p.E746_S752>V | 0.0035 |
c.2240_2254del15 | p.L747_T751del | 0.0033 |
c.2582T>A | p.L861Q | 0.0027 |
c.2239_2256del18 | p.L747_S752del | 0.0021 |
c.2155G>A | p.G719S | 0.0019 |
c.2303G>T | p.S768I | 0.0018 |
c.2156G>C | p.G719A | 0.0018 |
c.866C>T | p.A289V | 0.0016 |
c.2239_2253del15 | p.L747_T751del | 0.0015 |
c.2239_2251>C | p.L747_T751>P | 0.0015 |
c.2239_2247del9 | p.L747_E749del | 0.0014 |
c.2237_2251del15 | p.E746_T751>A | 0.0014 |
c.2155G>T | p.G719C | 0.0013 |
c.2497T>G | p.L833V | 0.0012 |
c.1793G>T | p.G598V | 0.0012 |
c.2125G>A | p.E709K | 0.0008 |
c.2307_2308insGCCAGCGTG | p.V769_D770insASV | 0.0007 |
c.2126A>C | p.E709A | 0.0007 |
c.2240_2251del12 | p.L747_T751>S | 0.0006 |
c.2239_2258>CA | p.L747_P753>Q | 0.0006 |
c.323G>A | p.R108K | 0.0005 |
c.89_889del801 | p.V30_R297>G | 0.0004 |
c.2203G>A | p.G735S | 0.0003 |
c.2238_2248>GC | p.L747_A750>P | 0.0003 |
c.2126A>G | p.E709G | 0.0003 |
c.2238_2255del18 | p.E746_S752>D | 0.0003 |
c.787A>C | p.T263P | 0.0003 |
c.865G>A | p.A289T | 0.0002 |
c.2126A>T | p.E709V | 0.0002 |
c.866C>A | p.A289D | 0.0002 |
c.2237_2252>T | p.E746_T751>V | 0.0002 |
c.2572C>A | p.L858M | 0.0002 |
c.2310_2311insGGT | p.D770_N771insG | 0.0002 |
c.2248G>C | p.A750P | 0.0002 |
c.2429G>A | p.G810D | 0.0002 |
c.2156G>A | p.G719D | 0.0002 |
c.2239_2256>CAA | p.L747_S752>Q | 0.0002 |
c.2193G>A | p.W731* | 0.0002 |
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