Kras 8 mutsations

An sami mawu a cikin kras gene na nau'ikan tsiro na ɗan adam, kusan 17% ~ kashi 30% ~ 50% maye gurbi a cikin cutar kansa marasa lafiya. Saboda furotin P21 wanda aka gina shi ta hanyar K-Ras shine geteryasashen Signing na hanyar Egfr, bayan da aka yi niyya da magungunan ƙasa akan Egfr, wanda ya haifar da ci gaba m yaduwar sel. Gashingen maye a cikin G-Ras Genear da tsayayya da cutar Egfr Tyrosine Kinaseors a cikin cututtukan ƙwayar cutar sankara a cikin cutar cututtukan daji na cutarwa. A shekara ta 2008, cibiyar sadarwa ta ƙasa ta ƙasa (NCCN) ta ba da izinin Cibiyar Ciniki ga cutar kansa ta 12 da 13 na Exon 2, kuma sun ba da shawarar hakan. Duk marasa lafiya da ke da cutar kansa mai coporic na cigaba na ƙwayoyin cuta a gaban K-RAS. Saboda haka, saurin gano matsalar K-Ras Ganewar shine na babban mahimmanci a cikin jagorar gargajiya. Wannan kit ɗin yana amfani da DNA kamar yadda samfurin gano zai samar da kimantawa game da yanayin maye gurbi, wanda ke taimaka wa darasin cutar kansa, mahaifa da sauran marasa lafiya da ke amfana daga kwayoyi masu niyya. Sakamakon gwajin na kit ɗin yana don tunani na asibiti kawai kuma bai kamata a yi amfani dashi azaman tushen kawai ga keɓaɓɓen magani ba. Calicians suyi hukunce-hukuncen gwaji game da sakamakon gwajin dangane da dalilai na haƙuri, martani da sauran alamomin dakin gwaje-gwaje.