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Exact(18)
SOD1 mutations were rare (0.83%), but a novel and probably disease-causing mutation was identified: p.Ala152Pro (c.457G>C).
CRC mutations were rare in the CLL cohort.
Interestingly, the TOR1 and TOR2 mutations were rare and dominant.
Sex provided no advantage in the permissive environment where beneficial mutations were rare.
Previous studies have shown that EGFR activating mutations were rare in ESCC.
Many mutations were rare or unique compared with the other genomes investigated.
Similar(42)
Unlike TP53, which is mutated in about 50 80% of human cancers, the TP73 gene mutations are rare.
And because most of the mutations are rare, they are extremely hard to find.
EGFR gene mutations are rare.
RAS mutations are rare except in MM and PCL.
SDHB and SDHD mutations are more common, whereas SDHA and SDHC mutations are rare.
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