Assertion list
mutation (primary) → ReceivesAction
Results from Ascent++: 308
mutation → ReceivesAction → inherited 0.66
mutation → ReceivesAction → shown in table 0.66
mutation → ReceivesAction → associated with resistance 0.66
mutation → ReceivesAction → confirmed 0.63
mutation → ReceivesAction → selected 0.63
mutation → ReceivesAction → confirmed by dna sequencing 0.62
mutation → ReceivesAction → confirmed by sanger sequencing 0.61
mutation → ReceivesAction → associated with disease 0.61
mutation → ReceivesAction → tested 0.61
mutation → ReceivesAction → favored by natural selection 0.59
mutation → ReceivesAction → identified 0.58
mutation → ReceivesAction → distributed 0.58
mutation → ReceivesAction → detected 0.58
mutation → ReceivesAction → removed 0.58
mutation → ReceivesAction → verified 0.57
mutation → ReceivesAction → identified in patient 0.57
mutation → ReceivesAction → reported 0.57
mutation → ReceivesAction → linked to breast cancer 0.56
mutation → ReceivesAction → studied 0.56
mutation → ReceivesAction → caused by mutagen 0.55
mutation → ReceivesAction → generated by site-directed muta… 0.55
mutation → ReceivesAction → shown 0.55
mutation → ReceivesAction → likely to occur 0.55
mutation → ReceivesAction → described 0.54
mutation → ReceivesAction → passed on to offspring 0.54
mutation → ReceivesAction → associated with cancer 0.53
mutation → ReceivesAction → inherited in autosomal dominant… 0.52
mutation → ReceivesAction → discovered 0.52
mutation → ReceivesAction → reported in patient 0.52
mutation → ReceivesAction → associated with drug resistance 0.52
mutation → ReceivesAction → associated with aml 0.51
mutation → ReceivesAction → described in the literature 0.51
mutation → ReceivesAction → associated with the disease 0.51
mutation → ReceivesAction → detected by direct sequencing 0.51
mutation → ReceivesAction → corrected 0.50
mutation → ReceivesAction → tolerated 0.50
mutation → ReceivesAction → identified by wes 0.50
mutation → ReceivesAction → identified in tumor 0.50
mutation → ReceivesAction → reversed 0.50
mutation → ReceivesAction → traced 0.50
mutation → ReceivesAction → linked to pd 0.49
mutation → ReceivesAction → confirmed by pcr 0.49
mutation → ReceivesAction → taken into account 0.49
mutation → ReceivesAction → introduced 0.49
mutation → ReceivesAction → associated with autism 0.49
mutation → ReceivesAction → linked to breast 0.48
mutation → ReceivesAction → added 0.48
mutation → ReceivesAction → predicted to be deleterious 0.48
mutation → ReceivesAction → removed by natural selection 0.47
mutation → ReceivesAction → identified to date 0.47
mutation → ReceivesAction → confirmed by dna sequence analy… 0.47
mutation → ReceivesAction → described in methods 0.47
mutation → ReceivesAction → associated to date 0.46
mutation → ReceivesAction → associated with inh resistance 0.46
mutation → ReceivesAction → associated with hearing loss 0.46
mutation → ReceivesAction → described to date 0.46
mutation → ReceivesAction → clustered in exon 0.46
mutation → ReceivesAction → fixed 0.45
mutation → ReceivesAction → common in the ashkenazi populat… 0.45
mutation → ReceivesAction → taken per four mutator levels 0.45
mutation → ReceivesAction → correlated with ovarian cancer 0.45
mutation → ReceivesAction → lost 0.45
mutation → ReceivesAction → caused by radiation 0.45
mutation → ReceivesAction → associated with sensitivity 0.45
mutation → ReceivesAction → observed 0.44
mutation → ReceivesAction → implicated 0.44
mutation → ReceivesAction → linked to schizophrenia 0.44
mutation → ReceivesAction → eliminated 0.44
mutation → ReceivesAction → identified in people 0.44
mutation → ReceivesAction → linked 0.44
mutation → ReceivesAction → predicted to be damaging 0.44
mutation → ReceivesAction → associated with mild phenotype 0.44
mutation → ReceivesAction → confirmed by bidirectional sequ… 0.44
mutation → ReceivesAction → detected by the kit 0.44
mutation → ReceivesAction → listed in additional file 0.44
mutation → ReceivesAction → validated by sanger 0.44
mutation → ReceivesAction → excluded 0.44
mutation → ReceivesAction → rejected 0.44
mutation → ReceivesAction → maintained in the population 0.42
mutation → ReceivesAction → detected at high frequency 0.42
mutation → ReceivesAction → involved in different families 0.42
mutation → ReceivesAction → written 0.42
mutation → ReceivesAction → associated with dwarfism 0.42
mutation → ReceivesAction → caused by dna damage 0.42
mutation → ReceivesAction → passed to child 0.42
mutation → ReceivesAction → underlined 0.41
mutation → ReceivesAction → associated with fmf 0.41
mutation → ReceivesAction → associated with starting protein 0.41
mutation → ReceivesAction → confirmed to be somatic 0.41
mutation → ReceivesAction → passed on to future generations 0.41
mutation → ReceivesAction → noted in red 0.41
mutation → ReceivesAction → caused by transposon 0.41
mutation → ReceivesAction → identified in gene 0.41
mutation → ReceivesAction → passed 0.40
mutation → ReceivesAction → seen in our cohort 0.40
mutation → ReceivesAction → missed 0.40
mutation → ReceivesAction → recognized 0.40
mutation → ReceivesAction → accumulated 0.40
mutation → ReceivesAction → induced by bcnu 0.40
mutation → ReceivesAction → induced by acnu 0.39
mutation → ReceivesAction → present in parent 0.39
mutation → ReceivesAction → reported in individual 0.39
mutation → ReceivesAction → caused by virus 0.39
mutation → ReceivesAction → required to cause disease 0.38
mutation → ReceivesAction → common in general population 0.38
mutation → ReceivesAction → caused by favipiravir 0.38
mutation → ReceivesAction → identified in 2014 0.38
mutation → ReceivesAction → associated with congenital cata… 0.38
mutation → ReceivesAction → likely to lead 0.38
mutation → ReceivesAction → mapped to chromosome 0.38
mutation → ReceivesAction → implicated in human 0.37
mutation → ReceivesAction → linked to leukemia 0.37
mutation → ReceivesAction → identified in lung adenocarcino… 0.37
mutation → ReceivesAction → shared 0.37
mutation → ReceivesAction → inherited in autosomal recessiv… 0.36
mutation → ReceivesAction → associated with alzheimer's dis… 0.36
mutation → ReceivesAction → associated with condition 0.35
mutation → ReceivesAction → associated with lymphedema 0.35
mutation → ReceivesAction → common in other tumor types 0.35
mutation → ReceivesAction → located on long arm of chromoso… 0.35
mutation → ReceivesAction → associated with poor prognosis 0.35
mutation → ReceivesAction → associated with other cancers 0.35
mutation → ReceivesAction → identified in proband 0.35
mutation → ReceivesAction → associated with poorer outcomes 0.34
mutation → ReceivesAction → associated with prostate 0.34
mutation → ReceivesAction → distributed throughout the gene 0.34
mutation → ReceivesAction → identified in atm 0.34
mutation → ReceivesAction → informative to identify and cla… 0.34
mutation → ReceivesAction → shown in fig 0.34
mutation → ReceivesAction → caused by chemical 0.34
mutation → ReceivesAction → expected 0.34
mutation → ReceivesAction → caused by error 0.33
mutation → ReceivesAction → a consequence of replication in… 0.33
mutation → ReceivesAction → associated with af 0.33
mutation → ReceivesAction → detected by ngs 0.33
mutation → ReceivesAction → released into a gene pool 0.33
mutation → ReceivesAction → scattered throughout the genome 0.33
mutation → ReceivesAction → accumulated over time 0.32
mutation → ReceivesAction → annotated 0.32
mutation → ReceivesAction → associated with ahus 0.32
mutation → ReceivesAction → associated with fh 0.32
mutation → ReceivesAction → associated with lgmd 0.32
mutation → ReceivesAction → caused by environmental factors 0.32
mutation → ReceivesAction → deemed random 0.32
mutation → ReceivesAction → detected in three patients 0.32
mutation → ReceivesAction → followed by loss of heterozygos… 0.32
mutation → ReceivesAction → implicated in pancreatic cancer 0.32
mutation → ReceivesAction → induced by new mutagenesis tech… 0.32
mutation → ReceivesAction → sequenced 0.32
mutation → ReceivesAction → shown on branch 0.32
mutation → ReceivesAction → caused by smoking 0.32
mutation → ReceivesAction → associated with diabetes 0.32
mutation → ReceivesAction → associated with lynch syndrome 0.32
mutation → ReceivesAction → associated with antimicrobial r… 0.31
mutation → ReceivesAction → carried by the patient 0.31
mutation → ReceivesAction → characterised by dominant or se… 0.31
mutation → ReceivesAction → color-coded 0.31
mutation → ReceivesAction → incorporated 0.31
mutation → ReceivesAction → likely to affect genes 0.31
mutation → ReceivesAction → likely to cause a radical change 0.31
mutation → ReceivesAction → masked by later ones 0.31
mutation → ReceivesAction → present in all affected living … 0.31
mutation → ReceivesAction → present in all of the body's ce… 0.31
mutation → ReceivesAction → caused by exposure 0.31
mutation → ReceivesAction → observed in brazil 0.29
mutation → ReceivesAction → shown in blue 0.29
mutation → ReceivesAction → treated with gefitinib 0.29
mutation → ReceivesAction → associated with increased risk 0.29
mutation → ReceivesAction → associated with acute myeloid l… 0.29
mutation → ReceivesAction → associated with frontotemporal … 0.29
mutation → ReceivesAction → correlated with colorectal 0.29
mutation → ReceivesAction → difficult to detect 0.29
mutation → ReceivesAction → associated with cardiomyopathy 0.28
mutation → ReceivesAction → associated with obesity 0.27
mutation → ReceivesAction → associated with alkaptonuria 0.27
mutation → ReceivesAction → associated with aniridia 0.27
mutation → ReceivesAction → associated with delayed parasit… 0.27
mutation → ReceivesAction → associated with first- and seco… 0.27
mutation → ReceivesAction → associated with gbm 0.27
mutation → ReceivesAction → associated with increased ovula… 0.27
mutation → ReceivesAction → associated with isoniazid resis… 0.27
mutation → ReceivesAction → associated with primary resista… 0.27
mutation → ReceivesAction → associated with renal cysts 0.27
mutation → ReceivesAction → associated with rifampicin resi… 0.27
mutation → ReceivesAction → carried by neoplastic clone 0.27
mutation → ReceivesAction → correlated 0.27
mutation → ReceivesAction → highlighted 0.27
mutation → ReceivesAction → involved in binding to csp 0.27
mutation → ReceivesAction → kept in check 0.27
mutation → ReceivesAction → limited 0.27
mutation → ReceivesAction → linked to cpvt 0.27
mutation → ReceivesAction → neglected 0.27
mutation → ReceivesAction → replicated 0.27
mutation → ReceivesAction → reported in the hgmd 0.27
mutation → ReceivesAction → responsible for alagille syndro… 0.27
mutation → ReceivesAction → shaded 0.27
mutation → ReceivesAction → never be avoided 0.27
mutation → ReceivesAction → discussed 0.25
mutation → ReceivesAction → acquired by smooth muscle cells 0.25
mutation → ReceivesAction → associated with antifolate resi… 0.25
mutation → ReceivesAction → associated with ars type 0.25
mutation → ReceivesAction → associated with benign genetic … 0.25
mutation → ReceivesAction → associated with cadasil syndrome 0.25
mutation → ReceivesAction → associated with crohn’s disease 0.25
mutation → ReceivesAction → associated with dcm 0.25
mutation → ReceivesAction → associated with familial hemipl… 0.25
mutation → ReceivesAction → associated with harp syndrome 0.25
mutation → ReceivesAction → associated with mesothelioma 0.25
mutation → ReceivesAction → associated with pcg 0.25
mutation → ReceivesAction → associated with pmf 0.25
mutation → ReceivesAction → buffered 0.25
mutation → ReceivesAction → carried by all 18 men 0.25
mutation → ReceivesAction → carried by related breeds 0.25
mutation → ReceivesAction → caused by cosmic rays 0.25
mutation → ReceivesAction → classified as level 0.25
mutation → ReceivesAction → classified into two groups 0.25
mutation → ReceivesAction → created at predefined points 0.25
mutation → ReceivesAction → detected at baseline 0.25
mutation → ReceivesAction → detected by d-hplc/ds 0.25
mutation → ReceivesAction → detected by hrm 0.25
mutation → ReceivesAction → detected by whole genome 0.25
mutation → ReceivesAction → discovered in 2013 0.25
mutation → ReceivesAction → easy to detect 0.25
mutation → ReceivesAction → enriched in tumor 0.25
mutation → ReceivesAction → found within large dna regions 0.25
mutation → ReceivesAction → fused in sarcoma 0.25
mutation → ReceivesAction → identified by exome sequencing 0.25
mutation → ReceivesAction → identified in 2009 0.25
mutation → ReceivesAction → identified in cataractogenesis 0.25
mutation → ReceivesAction → identified in patients of europ… 0.25
mutation → ReceivesAction → identified in to3 mouse mutant 0.25
mutation → ReceivesAction → induced by ethylnitrosourea 0.25
mutation → ReceivesAction → induced by gamma radiation 0.25
mutation → ReceivesAction → involved in the buildup of subs… 0.25
mutation → ReceivesAction → isolated in genetic screens 0.25
mutation → ReceivesAction → likely to be non 0.25
mutation → ReceivesAction → linked to dyskeratosis congenita 0.25
mutation → ReceivesAction → listed below the haplogroup name 0.25
mutation → ReceivesAction → made in single cycle of hiv-1 r… 0.25
mutation → ReceivesAction → needed to confer some ability 0.25
mutation → ReceivesAction → predicted by polyphen-2 0.25
mutation → ReceivesAction → present in two archaic samples 0.25
mutation → ReceivesAction → prioritized 0.25
mutation → ReceivesAction → propagated to new generations o… 0.25
mutation → ReceivesAction → reported in two other turkish f… 0.25
mutation → ReceivesAction → seen in two other children 0.25
mutation → ReceivesAction → selected in all of the evolutio… 0.25
mutation → ReceivesAction → shown above structural domains 0.25
mutation → ReceivesAction → subject to genetic drift 0.25
mutation → ReceivesAction → transmitted to large numbers of… 0.25
mutation → ReceivesAction → treated with erlotinib 0.25
mutation → ReceivesAction → unlinked 0.25
mutation → ReceivesAction → linked to depression 0.25
mutation → ReceivesAction → identified in affected individu… 0.24
mutation → ReceivesAction → indicated by asterisk 0.24
mutation → ReceivesAction → associated with immunodeficiency 0.24
mutation → ReceivesAction → correlated with gastric 0.24
mutation → ReceivesAction → correlated with thyroid 0.24
mutation → ReceivesAction → located on the x chromosome 0.24
mutation → ReceivesAction → seen in skeletal muscle 0.23
mutation → ReceivesAction → associated with atherosclerosis 0.22
mutation → ReceivesAction → associated with type 2 diabetes 0.22
mutation → ReceivesAction → determined by genetic test 0.22
mutation → ReceivesAction → linked to cardiovascular disease 0.22
mutation → ReceivesAction → never selected 0.22
mutation → ReceivesAction → associated with malignant hyper… 0.21
mutation → ReceivesAction → caused by physical agents 0.21
mutation → ReceivesAction → associated with metastasis 0.20
mutation → ReceivesAction → associated with ad 0.19
mutation → ReceivesAction → associated with survival 0.19
mutation → ReceivesAction → associated with asthma 0.19
mutation → ReceivesAction → associated with charcot-marie-t… 0.19
mutation → ReceivesAction → associated with hepatocellular … 0.19
mutation → ReceivesAction → associated with the cone-rod dy… 0.19
mutation → ReceivesAction → linked to lymphoma 0.19
mutation → ReceivesAction → detected in contrast 0.18
mutation → ReceivesAction → associated with artemisinin res… 0.17
mutation → ReceivesAction → associated with aggressive mast… 0.16
mutation → ReceivesAction → associated with altered distrib… 0.16
mutation → ReceivesAction → associated with angiogenesis 0.16
mutation → ReceivesAction → associated with autosomal domin… 0.16
mutation → ReceivesAction → associated with earlier onset o… 0.16
mutation → ReceivesAction → associated with elevated total … 0.16
mutation → ReceivesAction → associated with fluoroquinolone… 0.16
mutation → ReceivesAction → associated with long qt syndrome 0.16
mutation → ReceivesAction → associated with mastocytosis 0.16
mutation → ReceivesAction → associated with non-hodgkin lym… 0.16
mutation → ReceivesAction → associated with peripheral neur… 0.16
mutation → ReceivesAction → associated with reduced enzyme … 0.16
mutation → ReceivesAction → associated with sudden cardiac … 0.16
mutation → ReceivesAction → carried to actual genetic damage 0.16
mutation → ReceivesAction → caused by sunlight 0.16
mutation → ReceivesAction → detected on exosome rna 0.16
mutation → ReceivesAction → identified in skin lesions 0.16
mutation → ReceivesAction → linked with spontaneous, non-in… 0.16
mutation → ReceivesAction → predicted to be damaging by sift 0.16
mutation → ReceivesAction → reported in the abca1 gene 0.16
mutation → ReceivesAction → responsible for hirschsprung di… 0.16
mutation → ReceivesAction → used to profile fusion 0.16
mutation → ReceivesAction → used to profile splice variants 0.16
mutation → ReceivesAction → detected in rps14 0.15
mutation → ReceivesAction → identified by sequence analysis 0.15
mutation → ReceivesAction → associated with drug sensitivity 0.13
mutation → ReceivesAction → associated with poag 0.11
mutation → ReceivesAction → associated with lamivudine resi… 0.09
mutation → ReceivesAction → associated with nnrti resistance 0.09
mutation → ReceivesAction → identified by tes 0.09
mutation → ReceivesAction → identified in the tau gene 0.09