Incidental Mutations

45 incidental mutations are currently displayed, and affect 45 genes.
8 are Possibly Damaging.
16 are Probably Damaging.
16 are Probably Benign.
5 are Probably Null.
2 create premature stop codons.
1 are critical splice junction mutations.

Mutations in Coding Regions/Splice Sites Identified by Next-Gen Sequencing
[records 1 to 45 of 45] per page Full List
 
ID question?
Source question?
Gene question?
E-score question?
 
Stock # question?
Gen question?
Quality
-
Vld question?
Strain question?
Chr question?
Position question?
 
Mutation question?
Ref
Var
Type question?
Exon Dist question?
 
Zygosity question?
Predicted Effect question?
PPH Score question?
-
Meta Score question?
 
MGI Phenotype question?
Posted question?
 
1 293858 APN Abcc4 0.000 IGL02391 14 118553352 (GRCm38) N748Y T A missense Het probably damaging 1.000 phenotype 2015-04-16
2 293869 APN Actbl2 0.117 IGL02391 13 111255167 (GRCm38) D12G A G missense Het possibly damaging 0.614 2015-04-16
3 293845 APN Adamts10 0.320 IGL02391 17 33528811 (GRCm38) S74P T C missense Het probably benign 0.003 phenotype 2015-04-16
4 293874 APN Adprhl2 0.000 IGL02391 4 126317908 (GRCm38) C T splice site Het probably benign phenotype 2015-04-16
5 293873 APN Amn1 0.146 IGL02391 6 149169446 (GRCm38) A G critical splice donor site 2 bp Het probably null 2015-04-16
6 293843 APN Antxr1 0.000 IGL02391 6 87287056 (GRCm38) I144N A T missense Het probably damaging 1.000 phenotype 2015-04-16
7 293860 APN Atp2a3 0.113 IGL02391 11 72975339 (GRCm38) H262N C A missense Het probably benign 0.001 phenotype 2015-04-16
8 293867 APN Cabp5 0.000 IGL02391 7 13398344 (GRCm38) R13* A T nonsense Het probably null phenotype 2015-04-16
9 293859 APN Cacna1e 0.187 IGL02391 1 154421113 (GRCm38) Y1669H A G missense Het probably damaging 1.000 phenotype 2015-04-16
10 293852 APN Ccdc174 1.000 IGL02391 6 91898282 (GRCm38) E364G A G missense Het possibly damaging 0.719 phenotype 2015-04-16
11 293862 APN Ccdc18 0.000 IGL02391 5 108136052 (GRCm38) P74S C T missense Het probably damaging 0.999 2015-04-16
12 293856 APN Clec3a 0.072 IGL02391 8 114425500 (GRCm38) S82L C T missense Het probably benign 0.300 2015-04-16
13 293841 APN Cnih3 0.000 IGL02391 1 181406513 (GRCm38) D43G A G missense Het probably damaging 1.000 phenotype 2015-04-16
14 293847 APN Dpp10 0.000 IGL02391 1 123650358 (GRCm38) T128M G A missense Het probably damaging 0.983 phenotype 2015-04-16
15 293865 APN Edar 0.419 IGL02391 10 58628581 (GRCm38) F79I A T missense Het probably damaging 0.965 phenotype 2015-04-16
16 293851 APN Eif2ak4 0.000 IGL02391 2 118420791 (GRCm38) H199Q T A missense Het probably benign 0.186 phenotype 2015-04-16
17 293842 APN Fermt1 1.000 IGL02391 2 132941951 (GRCm38) L46P A G missense Het probably damaging 0.999 phenotype 2015-04-16
18 293876 APN Glipr1 0.058 IGL02391 10 111988894 (GRCm38) A G unclassified Het probably benign phenotype 2015-04-16
19 293839 APN Gsdmc 0.049 IGL02391 15 63803579 (GRCm38) N129S T C missense Het probably damaging 0.993 2015-04-16
20 293863 APN Ift88 1.000 IGL02391 14 57481414 (GRCm38) S619P T C missense Het possibly damaging 0.641 phenotype 2015-04-16
21 293864 APN Itga9 1.000 IGL02391 9 118850805 (GRCm38) V262E T A missense Het probably benign 0.188 phenotype 2015-04-16
22 293870 APN Med17 0.967 IGL02391 9 15277667 (GRCm38) R101* G A nonsense Het probably null phenotype 2015-04-16
23 293854 APN Mta1 0.000 IGL02391 12 113136583 (GRCm38) I688N T A missense Het possibly damaging 0.794 phenotype 2015-04-16
24 293833 APN Muc4 0.099 IGL02391 16 32752076 (GRCm38) R651S A T missense Het probably benign 0.413 phenotype 2015-04-16
25 293846 APN Olfr109 0.080 IGL02391 17 37466586 (GRCm38) P127S C T missense Het probably damaging 1.000 phenotype 2015-04-16
26 293861 APN Olfr1342 0.070 IGL02391 4 118690341 (GRCm38) L37P A G missense Het probably damaging 0.999 phenotype 2015-04-16
27 293834 APN Olfr824 0.083 IGL02391 10 130126904 (GRCm38) V51A A G missense Het possibly damaging 0.754 phenotype 2015-04-16
28 293850 APN Opcml 0.061 IGL02391 9 28675264 (GRCm38) I93V A G missense Het probably damaging 0.963 phenotype 2015-04-16
29 293875 APN Parg 1.000 IGL02391 14 32262681 (GRCm38) T G splice site Het probably null phenotype 2015-04-16
30 293835 APN Rps3a3 IGL02391 13 108670883 (GRCm38) A G intron Het probably benign 2015-04-16
31 293877 APN Safb 0.757 IGL02391 17 56600813 (GRCm38) T A splice site Het probably benign phenotype 2015-04-16
32 293836 APN Sat2 0.340 IGL02391 11 69622749 (GRCm38) C54F G T missense Het probably damaging 1.000 2015-04-16
33 293871 APN Scin 0.000 IGL02391 12 40077531 (GRCm38) Y420F T A missense Het probably benign 0.045 phenotype 2015-04-16
34 293844 APN Slc22a29 0.000 IGL02391 19 8169353 (GRCm38) S362T A T missense Het probably benign 0.127 2015-04-16
35 293838 APN Smchd1 0.814 IGL02391 17 71431259 (GRCm38) D537G T C missense Het probably null 1.000 phenotype 2015-04-16
36 293853 APN Spred3 0.000 IGL02391 7 29166405 (GRCm38) S126P A G missense Het probably benign 0.004 phenotype 2015-04-16
37 293866 APN Ssh1 0.000 IGL02391 5 113942517 (GRCm38) E951K C T missense Het probably damaging 0.999 phenotype 2015-04-16
38 293849 APN Ssmem1 0.075 IGL02391 6 30512442 (GRCm38) E28G A G missense Het possibly damaging 0.847 2015-04-16
39 293872 APN Stox1 0.240 IGL02391 10 62659676 (GRCm38) A T splice site Het probably benign phenotype 2015-04-16
40 293868 APN Syn3 0.000 IGL02391 10 86064906 (GRCm38) I373V T C missense Het probably benign 0.224 phenotype 2015-04-16
41 293837 APN Tecrl 0.239 IGL02391 5 83354827 (GRCm38) F58L A T missense Het probably benign 0.002 2015-04-16
42 293848 APN Trp53bp1 0.000 IGL02391 2 121202710 (GRCm38) N1655S T C missense Het possibly damaging 0.669 phenotype 2015-04-16
43 293857 APN Usp2 0.000 IGL02391 9 44091227 (GRCm38) Q147H G T missense Het probably damaging 1.000 phenotype 2015-04-16
44 293855 APN Usp24 0.000 IGL02391 4 106407129 (GRCm38) N1751K T A missense Het possibly damaging 0.598 phenotype 2015-04-16
45 293840 APN Wipf1 0.215 IGL02391 2 73434143 (GRCm38) D438V T A missense Het probably damaging 0.999 phenotype 2015-04-16
[records 1 to 45 of 45]