patient | 0.63 |
tumor | 0.56 |
cancer | 0.56 |
people | 0.56 |
melanoma | 0.55 |
child | 0.54 |
combination | 0.51 |
single family | 0.50 |
primary tumor | 0.48 |
cancer cells | 0.48 |
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occur in exon | 0.62 |
occur in codon | 0.59 |
occur in gene | 0.58 |
produce protein | 0.58 |
change single protein b… | 0.58 |
occur by chance | 0.57 |
occur in fact | 0.55 |
accumulate over time | 0.54 |
drive carcinogenesis | 0.54 |
enable mutant organism | 0.54 |
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reduction | 0.65 |
disease | 0.62 |
cystic fibrosis | 0.59 |
frameshift | 0.55 |
a loss of information | 0.49 |
loss of function | 0.48 |
rp | 0.48 |
condition | 0.46 |
syndrome | 0.44 |
mo | 0.44 |
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little effect | 0.63 |
effect | 0.62 |
same effect | 0.59 |
minor effect | 0.58 |
significant effect | 0.55 |
impact | 0.55 |
profound effects | 0.51 |
consequence | 0.50 |
deleterious effects | 0.49 |
negative effect | 0.46 |
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random | 0.77 |
neutral | 0.74 |
rare | 0.73 |
harmful | 0.69 |
heterozygous | 0.68 |
common | 0.66 |
novel | 0.65 |
somatic | 0.64 |
deleterious | 0.64 |
beneficial | 0.64 |
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cancer | 0.63 |
amino acid substitutions | 0.57 |
amino acid changes | 0.55 |
cancer development | 0.53 |
evolution | 0.53 |
a premature stop codon | 0.51 |
increase | 0.51 |
shift | 0.50 |
premature stop | 0.50 |
genomic instability | 0.49 |
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change | 0.72 |
permanent change | 0.61 |
sudden change | 0.29 |
single base changes | 0.25 |
a base-pair sequence ch… | 0.25 |
certainty | 0.25 |
clinical applications o… | 0.25 |
inherited | 0.66 |
shown in table | 0.66 |
associated with resista… | 0.66 |
confirmed | 0.63 |
selected | 0.63 |
confirmed by dna sequen… | 0.62 |
confirmed by sanger seq… | 0.61 |
associated with disease | 0.61 |
tested | 0.61 |
favored by natural sele… | 0.59 |
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occult infection | 0.25 |